Novel herbicides 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP2375898 A1 2011-10-19 [EP2375898]EP2375898 B1 2015-09-16 [EP2375898] / 2011-10-192015-09-16
申请号/申请日
2009EP-0765114 / 2009-12-09
发明人
TAYLOR JOHN BENJAMIN;WAILES JEFFREY STEVEN;JEANMART STEPHANE ANDRÉ MARIE;GOVENKAR MANGALA;
申请人
SYNGENTA;SYNGENTA PARTICIPATIONS;
主分类号
IPC分类号
A01N-043/08A01N-043/10A01N-043/36A01N-043/40A01N-043/42A01N-043/60A01N-043/64A01N-043/78A01N-043/80A01N-043/82A01N-043/84C07D-213/26C07D-213/50C07D-213/61C07D-213/64
摘要
(EP2375898) Compounds of the formula (I) wherein the substituents are as defined in claim 1, are suitable for use as herbicides.
机翻摘要
暂无翻译结果,您可以尝试点击头部的翻译按钮。
地址
代理人
代理机构
;
优先权号
2008GB-0022834 2008-12-15 2009WO-EP66712 2009-12-09
主权利要求
(EP2375898) 1. A compound of formula I (see diagramm) wherein G is hydrogen or an agriculturally acceptable metal, sulfonium, ammonium or latentiating group; R **1 is methyl, ethyl, n-propyl, isopropyl, cyclopropyl, halomethyl, haloethyl, vinyl, ethynyl, halogen, C 1-C 2alkoxy or C 1-C 2haloalkoxy; R **2 and R **3 are independently of each other hydrogen, methyl, ethyl, n-propyl, isopropyl, cyclopropyl, halomethyl, haloethyl, vinyl, propenyl, ethynyl, propynyl, halogen, C 1-C 2alkoxy, C 1-C 2haloalkoxy, optionally substituted aryl or optionally substituted heteroaryl; and wherein, in R **2 and R **3, when present, the optional substituents on aryl are selected, independently, from: halogen, nitro, cyano, rhodano, isothiocyanato, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxy(C 1-C 6) alkyl, C 2-C 6alkenyl, C 2-C 6haloalkenyl, C 2-C 6alkynyl, C 3-C 7cycloalkyl (itself optionally substituted with C 1-C 6alkyl or halogen), C 5-7cycloalkenyl (itself optionally substituted with C 1-C 6alkyl or halogen), hydroxy, C 1-C 10alkoxy, C 1-C 10alkoxy(C 1-C 10)alkoxy, tri(C 1-C 4)alkylsilyl(C 1-C 6)alkoxy, C 1-C 6alkoxycarbonyl(C 1-C 10)alkoxy, C 1-C 10haloalkoxy, aryl(C 1-C 4)alkoxy (where the aryl group is optionally substituted with halogen or C 1-C 6alkyl), C 3-C 7cycloalkyloxy (where the cycloalkyl group is optionally substituted with C 1-C 6alkyl or halogen), C 3-C 10alkenyloxy, C 3-C 10alkynyloxy, mercapto, C 1-C 10alkylthio, C 1-C 10haloalkylthio, aryl(C 1-C 4)alkylthio, C 3-C 7cycloalkylthio (where the cycloalkyl group is optionally substituted with C 1-C 6alkyl or halogen), tri(C 1-C 4)-alkylsilyl(C 1-C 6)alkylthio, arylthio, C 1-C 6alkylsulfonyl, C 1-C 6haloalkylsulfonyl, C 1-C 6alkylsulfinyl, C 1-C 6haloalkylsulfinyl, arylsulfonyl, tri(C 1-C 4)alkylsilyl, aryldi(C 1-C 4)alkylsilyl, C 1-C 4alkyldiarylsilyl, triarylsilyl, C 1-C 10alkylcarbonyl, HO 2C, C 1-C 10alkoxycarbonyl, aminocarbonyl, C 1-C 6alkylaminocarbonyl, di(C 1-C 6alkyl)-aminocarbonyl, N-(C 1-C 3 alkyl)-N-(C 1-C 3alkoxy)aminocarbonyl, C 1-C 6alkylcarbonyloxy, arylcarbonyloxy, di(C 1-C 6)alkylaminocarbonyloxy, aryl (itself optionally substituted with C 1-C 6alkyl or halogen), heterocyclyl (itself optionally substituted with C 1-C 6alkyl or halogen), aryloxy (where the aryl group is optionally substituted with C 1-C 6alkyl or halogen), heterocyclyloxy (where the heterocyclyl group is optionally substituted with C 1-C 6alkyl or halogen), amino, C 1-C 6alkylamino, di(C 1-C 6)alkylamino, C 1-C 6alkylcarbonylamino, N-(C 1-C 6)alkylcarbonyl-N-(C 1-C 6)alkylamino, or arylcarbonyl (where the aryl group is itself optionally substituted with halogen or C 1-C 6alkyl);  or two adjacent positions on an aryl system are cyclised to form a 5, 6 or 7 membered carbocyclic or heterocyclic ring, itself optionally substituted with halogen or C 1-C 6alkyl; and wherein, in R **2 and R **3, when present, the heteroaryl is optionally substituted by C 1-C 4alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, cyano, nitro, halogen, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl or C 1-C 3alkylsulfonyl; R **4 is methyl, ethyl, n-propyl, isopropyl, cyclopropyl, halomethyl, haloethyl, vinyl, propenyl, ethynyl, propynyl, halogen, C 1-C 2alkoxy or C 1-C 2haloalkoxy; and R **5, R **6, R **7, R **8 and R **9 are independently hydrogen, halogen, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxy, C 1-C 6haloalkoxy, C 2-C 6alkenyl, C 2-C 6haloalkenyl, C 2-C 6alkynyl, C 3-C 6alkenyloxy, C 3-C 6haloalkenyloxy, C 3-C 6alkynyloxy, C 3-C 6cycloalkyl, C 1-C 6alkylthio, C 1-C 6alkylsulfinyl, C 1-C 6alkylsulfonyl, C 1-C 6alkoxysulfonyl, C 1-C 6haloalkoxysulfonyl, cyano, nitro, phenyl, phenyl substituted by C 1-C 4alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, cyano, nitro, halogen, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl or C 1-C 3alkylsulfonyl, or heteroaryl or heteroaryl substituted by C 1-C 4alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, cyano, nitro, halogen, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl or C 1-C 3alkylsulfonyl; or R **6 and R **7 or R **8 and R **9 together with the carbon atoms to which they are attached form an optionally substituted carbocyclic ring, or a heterocyclyl optionally substituted by C 1-C 6alkyl or C 1-C 6haloalkyl; wherein a "carbocyclic ring" means a cycloalkyl or cycloalkenyl group; and wherein, when present, the optional substituents on cycloalkyl or cycloalkenyl are C 1-C 3alkyl; or R **5 and R **6 together form a bond; and HetAr is an heteroaryl or heteroaryl substituted by C 1-C 4alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, cyano, nitro, halogen, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl or C 1-C 3alkylsulfonyl; and wherein when G is a latentiating group then G is selected from the groups phenylC 1-C 8alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano or by nitro), heteroarylC 1-C 8alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3 alkylsulfonyl, halogen, cyano or by nitro), C 3-C 8alkenyl, C 3-C 8haloalkenyl, C 3-C 8alkynyl, C(X **a)-R **a, C(X **b)-X **c-R **b, C(X **d)-N(R **c)-R **d, -SO 2-R **e, -P(X **e)(R **f)-R **9 and CH 2-X **f-R **h; wherein X **a, X **b, X **c, X **d, X **e and X **f are independently of each other oxygen or sulfur; and wherein R **a is H, C 1-C 18alkyl, C 2-C 18alkenyl, C 2-C 18alkynyl, C 1-C 10haloalkyl, C 1-C 10cyanoalkyl, C 1-C 10nitroalkyl, C 1-C 10aminoalkyl, C 1-C 5alkylamino(C 1-C 5)alkyl, C 2-C 8dialkylamino(C 1-C 5)alkyl, C 3-C 7cycloalkyl(C 1-C 5)alkyl, C 1-C 5alkoxy(C 1-C 5)alkyl, C 3-C 5alkenyloxy(C 1-C 5)alkyl, C 1-C 5alkylthio(C 1-C 5)alkyl, C 1-C 5alkylsulfinyl(C 1-C 5)alkyl, C 1-C 5alkylsulfonyl(C 1-C 5)alkyl, C 2-C 8alkylideneaminoxy(C 1-C 5)alkyl, C 1-C 5alkylcarbonyl(C 1-C 5)alkyl, C 1-C 5alkoxycarbonyl(C 1-C 5)alkyl, aminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylaminocarbonyl(C 1-C 5)alkyl, C 2-C 8dialkylaminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylcarbonylamino(C 1-C 5)alkyl, N-(C 1-C 5)alkylcarbonyl-N-(C 1-C 5)alkylamino(C 1-C 5)alkyl, C 3-C 6trialkylsilyl(C 1-C 5)alkyl, phenyl(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), heteroaryl(C 1-C 5)alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), C 2-C 5haloalkenyl, C 3-C 8cycloalkyl; phenyl or phenyl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; or heteroaryl or heteroaryl substituted by C 1-C 3 alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro;  R **b is C 1-C 18alkyl, C 3-C 18alkenyl, C 3-C 18alkynyl, C 2-C 10haloalkyl, C 1-C 10cyanoalkyl, C 1-C 10nitroalkyl, C 2-C 10aminoalkyl, C 1-C 5alkylamino(C 1-C 5)alkyl, C 2-C 8dialkylamino(C 1-C 5)alkyl, C 3-C 7cycloalkyl(C 1-C 5)alkyl, C 1-C 5alkoxy(C 1-C 5)alkyl, C 3-C 5alkenyloxy(C 1-C 5)alkyl, C 3-C 5alkynyloxy(C 1-C 5)alkyl, C 1-C 5alkylthio(C 1-C 5)alkyl, C 1-C 5alkylsulfinyl(C 1-C 5)alkyl, C 1-C 5alkylsulfonyl(C 1-C 5)alkyl, C 2-C 8alkylideneaminoxy(C 1-C 5)alkyl, C 1-C 5alkylcarbonyl(C 1-C 5)alkyl, C 1-C 5alkoxycarbonyl(C 1-C 5)alkyl, aminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylaminocarbonyl(C 1-C 5)alkyl, C 2-C 8dialkylaminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylcarbonylamino(C 1-C 5)alkyl, N-(C 1-C 5)alkylcarbonyl-N-(C 1-C 5)alkylamino(C 1-C 5)alkyl, C 3-C 6trialkylsilyl(C 1-C 5)alkyl, phenyl(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3habatkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), heteroarylC 1-C 5alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkyl-thio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), C 3-C 5haloalkenyl, C 3-C 8cycloalkyl; phenyl or phenyl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; or heteroaryl or heteroaryl substituted by C 1-C 3 alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; and R **c and R **d are each independently of each other hydrogen, C 1-C 10alkyl, C 3-C 10alkenyl, C 3-C 10alkynyl, C 2-C 10haloalkyl, C 1-C 10cyanoalkyl, C 1-C 10nitroalkyl, C 1-C 10aminoalkyl, C 1-C 5alkylamino(C 1-C 5)alkyl, C 2-C 8dialkylamino(C 1-C 5)alkyl, C 3-C 7cycloalkyl(C 1-C 5)alkyl, C 1-C 5alkoxy(C 1-C 5)alkyl, C 3-C 5alkenyloxy(C 1-C 5)alkyl, C 3-C 5alkynyloxy(C 1-C 5)alkyl, C 1-C 5alkylthio(C 1-C 5)alkyl, C 1-C 5alkylsulfinyl(C 1-C 5)alkyl, C 1-C 5alkylsulfonyl(C 1-C 5)alkyl, C 2-C 8alkylideneaminoxy(C 1-C 5)alkyl, C 1-C 5alkylcarbonyl(C 1-C 5)alkyl, C 1-C 5alkoxycarbonyl(C 1-C 5)alkyl, aminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylaminocarbonyl(C 1-C 5)alkyl, C 2-C 8dialkylaminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylcarbonylamino(C 1-C 5)alkyl, N-(C 1-C 5)alkylcarbonyl-N-(C 2-C 5)alkylaminoalkyl, C 3-C 6trialkylsilyl(C 1-C 5)alkyl, phenyl(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), heteroaryl(C 1-C 5)alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), C 2-C 5haloalkenyl, C 3-C 8cycloalkyl; phenyl or phenyl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; heteroaryl or heteroaryl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; heteroarylamino or heteroarylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; diheteroarylamino or diheteroarylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; phenylamino or phenylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; diphenylamino or diphenylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; or C 3-C 7cycloalkylamino, di-C 3-C 7cycloalkylamino or C 3-C 7cycloalkoxy; or R **c and R **d may join together to form a 3-7 membered ring, optionally containing one heteroatom selected from O or S; and R **e is C 1-C 10alkyl, C 2-C 10alkenyl, C 2-C 10alkynyl, C 1-C 10haloalkyl, C 1-C 10cyanoalkyl, C 1-C 10nitroalkyl, C 1-C 10aminoalkyl, C 1-C 5alkylamino(C 1-C 5)alkyl, C 2-C 8dialkylamino(C 1-C 5)alkyl, C 3-C 7cycloalkyl(B 1-C 5)alkyl, C 1-C 5alkoxy(C 1-C 5)alkyl, C 3-C 5alkenyloxy(C 1-C 5)alkyl, C 3-C 5alkynyloxy(C 1-C 5)alkyl, C 1-C 5alkylthio(C 1-C 5)alkyl, C 1-C 5alkylsulfinyl(C 1-C 5)alkyl, C 1-C 5alkylsulfonyl(C 1-C 5)alkyl, C 2-C 8alkylideneaminoxy(C 1-C 5)alkyl, C 1-C 5alkylcarbonyl(C 1-C 5)alkyl, C 1-C 5alkoxycarbonyl(C 1-C 5)alkyl, aminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylam inocarbonyl(C 1-C 5)alkyl, C 2-C 8dialkylaminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylcarbonylamino(C 1-C 5)alkyl, N-(C 1-C 5)alkylcarbonyl-N-(C 1-C 5)alkylamino(C 1-C 5)alkyl, C 3-C 6trialkylsilyl(C 1-C 5)alkyl, phenyl(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), heteroaryl(C 1-C 5)alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), C 2-C 5haloalkenyl, C 3-C 8cycloalkyl; phenyl or phenyl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; heteroaryl or heteroaryl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; heteroarylamino or heteroarylamino substituted by C 1-C 3 alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; diheteroarylamino or diheteroarylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; phenylamino or phenylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; diphenylamino or diphenylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; or C 3-C 7cycloalkylamino, diC 3-C 7cycloalkylamino, C 3-C 7cycloalkoxy, C 1-C 10alkoxy, C 1-C 10haloalkoxy, C 1-C 5alkylamino or C 2-C 8dialkylamino; R **f and R **g are are each independently of each other C 1-C 10alkyl, C 2-C 10alkenyl, C 2-C 10alkynyl, C 1-C 10alkoxy, C 1-C 10haloalkyl, C 1-C 10cyanoalkyl, C 1-C 10nitroalkyl, C 1-C 10aminoalkyl, C 1-C 5alkylamino(C 1-C 5)alkyl, C 2-C 8dialkylamino(C 1-C 5)alkyl, C 3-C 7cycloalkyl(C 1-C 5)alkyl, C 1-C 5alkoxy(C 1-C 5)alkyl.  C 3-C 5alkenyloxy(C 1-C 5)alkyl, C 3-C 5alkynyloxy(C 1-C 5)alkyl, C 1-C 5alkylthio(C 1-C 5)alkyl, C 1-C 5alkylsulfinyl(C 1-C 5)alkyl, C 1-C 5alkylsulfonyl(C 1-C 5)alkyl, C 2-C 8alkylideneaminoxy(C 1-C 5)alkyl, C 1-C 5alkylcarbonyl(C 1-C 5)alkyl, C 1-C 5alkoxycarbonyl(C 1-C 5)alkyl, aminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylaminocarbonyl(C 1-C 5)alkyl, C 2-C 8dialkylaminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylcarbonylamino(C 1-C 5)alkyl, N-(C 1-C 5)alkylcarbonyl-N-(C 2-C 5)alkylaminoalkyl, C 3-C 6trialkylsilyl(C 1-C 5)alkyl, phenyl(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), heteroaryl(C 1-C 5)alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3alkylsulfonyl, halogen, cyano, or by nitro), C 2-C 5haloalkenyl, C 3-C 8cycloalkyl; phenyl or phenyl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; heteroaryl or heteroaryl substituted by C 1-C 3 alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; heteroarylamino or heteroarylamino substituted by C 1-C 3 alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; diheteroarylamino or diheteroarylamino substituted by C 1-C3 alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; phenylamino or phenylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; diphenylamino or diphenylamino substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; or C 3-C 7cycloalkylamino, diC 3-C 7cycloalkylamino, C 3-C 7cycloalkoxy, C 1-C 10haloalkoxy, C 1-C 5alkylamino or C 2-C 8dialkylamino; or benzyloxy or phenoxy, wherein the benzyl and phenyl groups may in turn be substituted by C 1-C 3alkyl, C 1-C 3hatoalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or nitro; and R **h is C 1-C 10alkyl, C 3-C 10alkenyl, C 3-C 10alkynyl, C 1-C 10haloalkyl, C 1-C 10cyanoalkyl, C 1-C 10nitroalkyl, C 2-C 10aminoalkyl, C 1-C 5alkylamino(C 1-C 5)alkyl, C 2-C 8dialkylamino(C 1-C 5)alkyl, C 3-C 7cycloalkyl(C 1-C 5)alkyl, C 1-C 5alkoxy(C 1-C 5)alkyl, C 3-C 5alkenyloxy(C 1-C 5)alkyl, C 3-C 5alkynyloxy(C 1-C 5)alkyl, C 1-C 5alkylthio(C 1-C 5)alkyl, C 1-C 5alkylsulfinyl(C 1-C 5)alkyl, C 1-C 5alkylsulfonyl(C 1-C 5)alkyl, C 2-C 8alkylideneaminoxy(C 1-C 5)alkyl, C 1-C 5alkylcarbonyl(C 1-C 5)alkyl, C 1-C 5alkoxycarbonyl(C 1-C 5)alkyl, aminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylaminocarbonyl(C 1-C 5)alkyl, C 2-C 8dialkylaminocarbonyl(C 1-C 5)alkyl, C 1-C 5alkylcarbonylamino(C 1-C 5)alkyl, N-(C 1-C 5)alkylcarbonyl-N-(C 1-C 5)alkylamino(C 1-C 5)alkyl, C 3-C 6trialkylsilyl(C 1-C 5)alkyl, phenyl(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3 alkylsulfonyl, halogen, cyano or by nitro), heteroaryl(C 1-C 5)alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3 alkylsulfonyl, halogen, cyano or by nitro), phenoxy(C 1-C 5)alkyl (wherein the phenyl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3 alkylsulfonyl, halogen, cyano or by nitro), heteroaryloxy(C 1-C 5)alkyl (wherein the heteroaryl is optionally substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, C 1-C 3alkylthio, C 1-C 3alkylsulfinyl, C 1-C 3 alkylsulfonyl, halogen, cyano or by nitro), C 3-C 5haloalkenyl, C 3-C 8cycloalkyl; phenyl or phenyl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen or by nitro; or heteroaryl, or heteroaryl substituted by C 1-C 3alkyl, C 1-C 3haloalkyl, C 1-C 3alkoxy, C 1-C 3haloalkoxy, halogen, cyano or by nitro; and wherein "aryl" means phenyl; wherein "heteroaryl" means a 6-membered heteroaryl ring which is optionally benzannellated; and  wherein "heterocyclyl" means a non-aromatic monocyclic or bicyclic ring system containing up to 7 atoms including one or two heteroatoms selected from O, S and N. 2. A compound according to claim 1, wherein "heteroaryl" means pyridyl, pyrimidinyl, pyridazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl or quinoxalinyl. 3. A compound according to claim 1, wherein: "cycloalkyl" is cyclopropyl, cyclobutyl, cyclopentyl or cyclohexyl; "cycloalkylalkyl" is cyclopropylmethyl; and "cycloalkenyl" is cyclopentenyl or cyclohexenyl. 4. A compound according to claim 1, wherein  R **1 is methyl, ethyl, n-propyl, vinyl, ethynyl, halogen, C 1-C 2alkoxy or C 1-C 2haloalkoxy;  R **2 is methyl, halogen, C 1-C 2alkoxy or C 1-C 2haloalkoxy, or optionally substituted phenyl;  R **3 is hydrogen;  R **4 is methyl, ethyl, n-propyl, vinyl, ethynyl or methoxy; and  R **5, R **6, R **7, R **8 and R **9 are independently hydrogen, halogen, C 1-C 4alkyl, C 1-C 4haloalkyl, C 1-C 4alkoxy, C 1-C 4haloalkoxy, C 2-C 4alkenyl, C 2-C 4haloalkenyl, or C 2-C 4alkynyl; or  R **6 and R **7 or R **8 and R **9 together with the carbon atoms to which they are attached form an optionally substituted carbocyclic ring as defined in claim 1 or or an optionally substituted heterocyclyl as defined in claim 1; or  R **5 and R **6 together form a bond; and  HetAr is the heteroaryl or the heteroaryl substituted one to three times by fluoro, chloro, bromo, methyl, methoxy, cyano or trifluoromethyl. 5. A compound according to claim 4, wherein  R **1 is methyl or ethyl, R **2 is methyl or chloro, R **3 is hydrogen, and R **4 is methyl, ethyl or methoxy, and R **5, R **6, R **7, R **8 and R **9 are hydrogen, or R **5 and R **6 together form a bond; and  HetAr is a 6-membered heteroaryl or is a 6-membered heteroaryl which is substituted one to three times by fluoro, chloro, bromo, methyl, methoxy, cyano or trifluoromethyl. 6. A compound according to claim 1, 4 or 5, wherein HetAr is pyridyl, pyrimidinyl, pyridazinyl, quinolinyl, isoquinolinyl, cinnolinyl, phthalazinyl, quinazolinyl or quinoxalinyl, where these rings are optionally substituted one or two times by fluoro, chloro, bromo, methyl, methoxy, cyano or trifluoromethyl. 7. A compound according to claim 1, wherein, when G is a latentiating group, then G is a group - C(X **a)-R **a or -C(X **b)-X **c-R **b, and the meanings of X **a, R **a, X **b, X **c and R **b are as defined in claim 1. 8. A compound according to claim 1, wherein G is hydrogen. 9. A compound according to claim 1, which is one of the following compounds: (see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm) 10. A compound according to claim 1, which is a compound of structural type T-1: (see diagramm)wherein R **5, R **6, R **7, R **8 and R **9 are H; and wherein HetAr is 2-pyridyl, 3-fluoro-2-pyridyl, 4-fluoro-2-pyridyl, 5-fluoro-2-pyridyl, 6-fluoro-2-pyridyl, 3-chloro-2-pyridyl, 4-chloro-2-pyridyl, 5-chloro-2-pyridyl, 6-chloro-2-pyridyl, 3-methyl-2-pyridyl, 4-methyl-2-pyridyl, 5-methyl-2-pyridyl, 6-methyl-2-pyridyl, 3-trifluoromethyl-2-pyridyl, 4-trifluoromethyl -2-pyridyl, 5-trifluoromethyl -2-pyridyl, 6-trifluoromethyl -2-pyridyl, 3-methoxy-2-pyridyl, 4-methoxy-2-pyridyl, 5-methoxy-2-pyridyl, 6-methoxy-2-pyridyl, 3-trifluoromethoxy-2-pyridyl, 4-trifluoromethoxy-2-pyridyl, 5-trifluoromethoxy-2-pyridyl, 6-trifluoromethoxy-2-pyridyl, 3-cyano-2-pyridyl, 4-cyano-2-pyridyl, 5-cyano-2-pyridyl, 6-cyano-2-pyridyl, 3-nitro-2-pyridyl, 4-nitro-2-pyridyl, 5-nitro-2-pyridyl, 6-nitro-2-pyridyl, 3-methanesulfonyl-2-pyridyl, 4-methanesulfonyl-2-pyridyl, 5-methanesulfonyl-2-pyridyl, 6-methanesulfonyl-2-pyridyl, 3-pyridyl, 2-fluoro-3-pyridyl, 4-fluoro-3-pyridyl, 5-fluoro-3-pyridyl, 6-fluoro-3-pyridyl, 2-chloro-3-pyridyl, 4-chloro-3-pyridyl, 5-chloro-3-pyridyl, 6-chloro-3-pyridyl, 2-bromo-3-pyridyl, 4-bromo-3-pyridyl, 5-bromo-3-pyridyl, 6-bromo-3-pyridyl, 2-methoxy-3-pyridyl, 4-methoxy-3-pyridyl, 5-methoxy-3-pyridyl, 6-methoxy-3-pyridyl, 2-trifluoromethoxy-3-pyridyl, 4-trifluoromethoxy-3-pyridyl, 5-trifluoromethoxy-3-pyridyl, 6-trifluoromethoxy-3-pyridyl, 2-methyl-3-pyridyl, 4-methyl-3-pyridyl, 5-methyl-3-pyridyl, 6-methyl-3-pyridyl, 2-trifluoromethyl-3-pyridyl, 4-trifluoromethyl-3-pyridyl, 5- trifluoromethyl-3-pyridyl, 6-trifluoromethyl-3-pyridyl, 2-cyano-3-pyridyl, 4-cyano-3-pyridyl, 5-cyano-3-pyridyl, 6-cyano-3-pyridyl, 2-nitro-3-pyridyl, 4-nitro-3-pyridyl, 5-nitro-3-pyridyl, 6-nitro-3-pyridyl, 2-methanesulfonyl-3-pyridyl, 4-methanesulfonyl-3-pyridyl, 5-methanesulfonyl-3-pyridyl, 6-methanesulfonyl-3-pyridyl, 4-pyridyl, 2-fluoro-4-pyridyl, 3-fluoro-4-pyridyl, 2-chloro-4-pyridyl, 3-chloro-4-pyridyl, 2-bromo-4-pyridyl, 3-bromo-4-pyridyl, 2-methoxy-4-pyridyl, 3-methoxy-4-pyridyl, 2-trifluoromethoxy-4-pyridyl, 3-trifluoromethoxy-4-pyridyl, 2-methyl-4-pyridyl, 3-methyl-4-pyridyl, 2-trifluoromethyl-4-pyridyl, 3-trifluoromethyl-4-pyridyl, 2-cyano-4-pyridyl, 3-cyano-4-pyridyl, 2-nitro-4-pyridyl, 3-nitro-4-pyridyl, 2-methanesulfonyl-4-pyridyl, 3- methanesulfonyl-4-pyridyl, 2-pyridazinyl, 4-fluoro-2-pyridazinyl, 5-fluoro-2-pyridazinyl, 6-fluoro-2-pyridazinyl, 4-chloro-2-pyridazinyl, 5-chloro-2-pyridazinyl, 6-chloro-2-pyridazinyl, 4-bromo-2-pyridazinyl, 5-bromo-2-pyridazinyl, 6-bromo-2-pyridazinyl, 4-methoxy-2-pyridazinyl, 5-methoxy-2-pyridazinyl, 6-methoxy-2-pyridazinyl, 4-trifluoromethoxy-2-pyridazinyl, 5-trifluoromethoxy-2-pyridazinyl, 6-trifluoromethoxy-2-pyridazinyl, 4-methyl-2-pyridazinyl, 5-methyl-2-pyridazinyl, 6-methyl-2-pyridazinyl, 4-trifluoromethyl-2-pyridazinyl, 5-trifluoromethyl-2-pyridazinyl, 6-trifluoromethyl-2-pyridazinyl, 4-cyano-2-pyridazinyl, 5-cyano-2-pyridazinyl, 6-cyano-2-pyridazinyl, 4-nitro-2-pyridazinyl, 5-nitro-2-pyridazinyl, 6-nitro-2-pyridazinyl, 4-methanesulfonyl-2-pyridazinyl, 5-methanesulfonyl-2-pyridazinyl, 6-methanesulfonyl-2-pyridazinyl, 3-pyridazinyl, 2-fluoro-3-pyridazinyl, 5-fluoro-3-pyridazinyl, 6-fluoro-3-pyridazinyl, 2-chloro-3-pyridazinyl, 5-chloro-3-pyridazinyl, 6-chloro-3-pyridazinyl, 2-bromo-3-pyridazinyl, 5-bromo-3-pyridazinyl, 6-bromo-3-pyridazinyl, 2-methoxy-3-pyridazinyl, 5-methoxy-3-pyridazinyl, 6-methoxy-3-pyridazinyl, 2-trifluoromethoxy-3-pyridazinyl, 5-trifluoromethoxy-3-pyridazinyl, 6-trifluoromethoxy-3-pyridazinyl, 2-methyl-3-pyridazinyl, 5-methyl-3-pyridazinyl, 6-methyl-3-pyridazinyl, 2-trifluoromethyl-3-pyridazinyl, 5-trifluoromethyl-3-pyridazinyl, 6-trifluoromethyl-3-pyridazinyl, 2-cyano-3-pyridazinyl, 5-cyano-3-pyridazinyl, 6-cyano-3-pyridazinyl, 2-nitro-3-pyridazinyl, 5-nitro-3-pyridazinyl, 6-nitro-3-pyridazinyl, 2-methanesulfonyl-3-pyridazinyl, 5-methanesulfonyl-3-pyridazinyl, 6-methanesulfonyl-3-pyridazinyl, 2-pyrimidyl, 4-fluoro-2-pyrimidyl, 5-fluoro-2-pyrimidyl, 4-chloro-2-pyrimidyl, 5-chloro-2-pyrimidyl, 4-bromo-2-pyrimidyl, 5-bromo-2-pyrimidyl, 4-methoxy-2-pyrimidyl, 5-methoxy-2-pyrimidyl, 4-trifluoromethoxy-2-pyrimidyl, 5-trifluoromethoxy-2-pyrimidyl, 4-methyl-2-pyrimidyl, 5-methyl-2-pyrimidyl, 4-trifluoromethyl-2-pyrimidyl, 5-trifluoromethyl-2-pyrimidyl, 4-cyano-2-pyrimidyl, 5-cyano-2-pyrimidyl, 4-nitro-2-pyrimidyl, 5-nitro-2-pyrimidyl, 4-methanesulfonyl-2-pyrimidyl, 5-methanesulfonyl-2-pyrimidyl, 4-pyrimidyl, 2-fluoro-4-pyrimidyl, 5-fluoro-4-pyrimidyl, 6-fluoro-4-pyrimidyl, 2-chloro-4-pyrimidyl, 5-chloro-4-pyrimidyl, 6-chloro-4-pyrimidyl, 2-bromo-4-pyrimidyl, 5-bromo-4-pyrimidyl, 6-bromo-4-pyrimidyl, 2-methoxy-4-pyrimidyl, 5-methoxy-4-pyrimidyl, 6-methoxy-4-pyrimidyl, 2-trifluoromethoxy-4-pyrimidyl, 5-trifluoromethoxy-4-pyrimidyl, 6-trifluoromethoxy-4-pyrimidyl, 2-methyl-4-pyrimidyl, 5-methyl-4-pyrimidyl, 6-methyl-4-pyrimidyl, 2-trifluoromethyl-4-pyrimidyl, 5-trifluoromethyl-4-pyrimidyl, 6-trifluoromethyl-4-pyrimidyl, 2-cyano-4-pyrimidyl, 5-cyano-4-pyrimidyl, 6-cyano-4-pyrimidyl, 2-nitro-4-pyrimidyl, 5-nitro-4-pyrimidyl, 6-nitro-4-pyrimidyl, 2-methanesulfonyl-4-pyrimidyl, 5-methanesulfonyl-4-pyrimidyl, 6-methanesulfonyl-4-pyrimidyl, 5-pyrimidyl, 2-fluoro-5-pyrimidyl, 4-fluoro-5-pyrimidyl, 2-chloro-5-pyrimidyl, 4-chloro-5-pyrimidyl, 2-bromo-5-pyrimidyl, 4-bromo-5-pyrimidyl, 2-methoxy-5-pyrimidyl, 4-methoxy-5-pyrimidyl, 2-trifluoromethoxy-5-pyrimidyl, 4-trifluoromethoxy-5-pyrimidyl, 2-methyl-5-pyrimidyl, 4-methyl-5-pyrimidyl, 2-trifluoromethyl-5-pyrimidyl, 4-trifluoromethyl-5-pyrimidyl, 2-cyano-5-pyrimidyl, 4-cyano-5-pyrimidyl, 2-nitro-5-pyrimidyl, 4-nitro-5-pyrimidyl, 2-methanesulfonyl-5-pyrimidyl, 4-methanesulfonyl-5-pyrimidyl, 2-pyrazinyl, 3-fluoro-2-pyrazinyl, 5-fluoro-2-pyrazinyl, 6-fluoro-2-pyrazinyl, 3-chloro-2-pyrazinyl, 5-chloro-2-pyrazinyl, 6-chloro-2-pyrazinyl, 3-bromo-2-pyrazinyl, 5-bromo-2-pyrazinyl, 6-bromo-2-pyrazinyl, 3-methoxy-2-pyrazinyl, 5-methoxy-2-pyrazinyl, 6-methoxy-2-pyrazinyl, 3-trifluoromethoxy-2-pyrazinyl, 5-trifluoromethoxy-2-pyrazinyl, 6-trifluoromethoxy-2-pyrazinyl, 3-methyl-2-pyrazinyl, 5-methyl-2-pyrazinyl, 6-methyl-2-pyrazinyl, 3-trifluoromethyl-2-pyrazinyl, 5-trifluoromethyl-2-pyrazinyl, 6-trifluoromethyl-2-pyrazinyl, 3-cyano-2-pyrazinyl, 5-cyano-2-pyrazinyl, 6-cyano-2-pyrazinyl, 3-nitro-2-pyrazinyl, 5-nitro-2-pyrazinyl, 6-nitro-2-pyrazinyl, 3-methylsulfonate-2-pyrazinyl, 5-methylsulfonate-2-pyrazinyl, or 6-methylsulfonate-2-pyrazinyl; and wherein: R **1, R **2 and R **4 are methyl and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is chloride and R **3 is hydrogen; or R **1 and R **2 are methyl, R **4 is chloride and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is bromide and R **3 is hydrogen; or R **1 is methyl, R **2 is chloride, R **3 is hydrogen, and R **4 is methoxy; or R **1 is methyl, R **2 is bromide, R **3 is hydrogen, and R **4 is methoxy; or R **1 and R **2 are methyl, R **4 is ethenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is ethynyl, and R **3 is hydrogen; or R **1 and R **2 are methyl, R **4 is ethynyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3-fluoro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3-chloro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3-trifluoro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 4-fluoro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 4-chloro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 4-trifluoro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3,4-difluoro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3-fluoro-4-chloro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3-chloro-4-fluoro-phenyl, and R **3 is hydrogen; or R **1 and R **4 are methyl, R **2 is 3,4-dichloro-phenyl, and R **3 is hydrogen; or R **1 is ethyl, R **2 and R **4 are methyl and R **3 is hydrogen;  or R **1 is ethyl, R **4 is methyl, R **2 is chloride and R **3 is hydrogen; or R **1 is ethyl, R **2 is methyl, R **4 is chloride and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is bromide and R **3 is hydrogen; or R **1 is ethyl, R **2 is chloride, R **3 is hydrogen, and R **4 is methoxy; or R **1 is ethyl, R **2 is bromide, R **3 is hydrogen, and R **4 is methoxy; or R **1 is ethyl, R **2 is methyl, R **4 is ethenyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 are methyl, R **2 is ethynyl, and R **3 is hydrogen; or R **1 is ethyl, R **2 is methyl, R **4 is ethynyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is phenyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is 3-fluoro-phenyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is 3-chloro-phenyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is 3-trifluoro-phenyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is 4-fluoro-phenyl, and R **3 is hydrogen; or R **1 is ethyl, R **4 is methyl, R **2 is 4-chloro-phenyl, and R(...)
法律状态
(EP2375898) LEGAL DETAILS FOR EP2375898  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED     Event publication date=2009-12-09  Event code=EP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=EP EP09765114  Application date=2009-12-09  Standardized application number=2009EP-0765114     Event publication date=2011-10-19  Event code=EP/A1  Event type=Examination events  Application published with search report  Publication country=EP  Publication number=EP2375898  Publication stage Code=A1  Publication date=2011-10-19  Standardized publication number=EP2375898     Event publication date=2011-10-19  Event code=EP/17P  Event indicator=Pos  Event type=Examination events  Request for examination filed Pruefungsantrag gestellt  Effective date of the event=2011-07-15     Event publication date=2011-10-19  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR    Event publication date=2011-10-19  Event code=EP/AX  Event indicator=Pos  Event type=Designated states  Extension of the European patent to Request for extension of the european patent to BA RS    Event publication date=2012-03-21  Event code=EP/RAX  Event type=Designated states  Event type=Corrections  Extension of the European patent to (correction) Requested extension states of the european patent have changed   Annual fees payment date=2012-03-21     BA RS    Event publication date=2012-07-04  Event code=EP/17Q  Event indicator=Pos  Event type=Examination events  First examination report Erster pruefungsbescheid  Effective date of the event=2012-06-05     Event publication date=2015-04-29  Event code=EP/INTG  Event indicator=Pos  Event type=Examination events  Announcement of intention to grant  Effective date of the event=2015-04-07     Event publication date=2015-09-16  Event code=EP/B1  Event indicator=Pos  Event type=Event indicating In Force  Patent specification  Publication country=EP  Publication number=EP2375898  Publication stage Code=B1  Publication date=2015-09-16  Standardized publication number=EP2375898     Event publication date=2015-09-16  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE BG CH CY CZ DE DK EE ES FI FR GB GR HR HU IE IS IT LI LT LU LV MC MK MT NL NO PL PT RO SE SI SK SM TR    Event publication date=2015-09-16  Event code=EP/AX  Event indicator=Pos  Event type=Designated states  Extension of the European patent to Request for extension of the european patent to BA RS    Event publication date=2016-08-24  Event code=EP/26N  Event indicator=Pos  Event type=No opposition filed  Event type=Event indicating In Force  No opposition filed Kein einspruch eingelegt  Effective date of the event=2016-06-17  MEMBER STATE LEGAL DETAILS FOR AT  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=AT Corresponding appl: AT749030    Event publication date=2015-10-15  Event code=EP/REG  Event code=AT/REF  Event indicator=Pos  Event type=Entry into national phase  Reference to a national code Reference to at number (ep patent enters austrian national phase) Nennung der e-nummer (ep patent tritt in at nationale phase ein) Corresponding cc:  Designated or member state=AT   Effective date of the event=2015-10-15     Event publication date=2017-07-15  Event code=EP/REG  Event code=AT/UEP  Event indicator=Pos  Event type=Examination events  Event type=Entry into national phase  Reference to a national code Publication of translation of european patent specification Uebersetzung der europaeischen patentschrift ausgegeben Corresponding cc:  Designated or member state=AT   Effective date of the event=2015-09-16     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=AT  MEMBER STATE LEGAL DETAILS FOR BE  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=BE     Event publication date=2017-12-13  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-13     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=BE  MEMBER STATE LEGAL DETAILS FOR BG  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=BG     Event publication date=2017-11-15  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-15     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=BG  MEMBER STATE LEGAL DETAILS FOR CH  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=CH     Event publication date=2015-09-30  Event code=EP/REG  Event code=CH/EP  Event indicator=Pos  Event type=Entry into national phase  Reference to a national code Entry in the national phase Eintritt in die nationale phase Corresponding cc:  Designated or member state=CH     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=CH  MEMBER STATE LEGAL DETAILS FOR CY  Actual or expected expiration date=2017-06-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CY     Event publication date=2017-06-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=CY  MEMBER STATE LEGAL DETAILS FOR CZ  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=CZ     Event publication date=2017-11-27  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-27     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=CZ  MEMBER STATE LEGAL DETAILS FOR DE  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=DE Corresponding appl: DE602009033690    Event publication date=2015-11-05  Event code=EP/REG  Event code=DE/R096  Event indicator=Pos  Event type=Examination events  Reference to a national code DPMA publication of mentioned EP patent grant Veroeffentlichung eines hinweises auf die ep-patenterteilung durch das dpma Corresponding cc:  Designated or member state=DE     Event publication date=2016-06-17  Event code=EP/REG  Event code=DE/R097  Event indicator=Pos  Event type=No opposition filed  Reference to a national code No opposition filed against granted patent, or EPO opposition proceedings concluded without decision Gegen die patenterteilung wurde kein einspruch erhoben, bzw. einspruchsverfahren ist beim epa ohne entscheidung abgeschlossen Corresponding cc:  Designated or member state=DE     Event publication date=2017-12-21  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-21     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=DE  MEMBER STATE LEGAL DETAILS FOR DK2375898  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=DK Corresponding appl: DK09765114  Application date in the designated or member state=2009-12-09   Application number in the designated or member state=2009DK-0765114 Corresponding cc:  Designated or member state=DK Corresponding pat: DK2375898  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2015-12-07   Publication number in the designated or member state=DK2375898T    Event publication date=2015-12-07  Event code=EP/REG  Event code=DK/T3  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Translation of EP patent Corresponding cc:  Designated or member state=DK   Effective date of the event=2015-12-01     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=DK  MEMBER STATE LEGAL DETAILS FOR EE  Actual or expected expiration date=2016-04-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=EE     Event publication date=2016-04-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=EE  MEMBER STATE LEGAL DETAILS FOR EP2997824  Actual or expected expiration date=2017-10-03    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=EP Corresponding appl: EP15179973  Application date in the designated or member state=2009-12-09   Application number in the designated or member state=2015EP-0179973 Corresponding cc:  Designated or member state=EP Corresponding pat: EP2997824  Publication stage code in the designated or member state=A1  Publication date in the designated or member state=2016-03-23   Publication number in the designated or member state=EP2997824    Event publication date=2018-03-07  Event code=EP/STCHG  Patent status changed by the national office Corresponding cc:  Designated or member state=EP  MEMBER STATE LEGAL DETAILS FOR ES2553417  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=ES Corresponding appl: ES09765114  Application date in the designated or member state=2009-12-09   Application number in the designated or member state=2009ES-0765114T Corresponding cc:  Designated or member state=ES Corresponding pat: ES2553417  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2015-12-09   Publication number in the designated or member state=ES2553417    Event publication date=2015-12-09  Event code=EP/REG  Event code=ES/FG2A  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Definitive protection Proteccion definitiva Corresponding cc:  Designated or member state=ES   Effective date of the event=2015-12-09     Event publication date=2018-01-05  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2018-01-05     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=ES  MEMBER STATE LEGAL DETAILS FOR FI  Actual or expected expiration date=2016-01-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=FI     Event publication date=2016-01-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=FI  MEMBER STATE LEGAL DETAILS FOR FR  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=FR     Event publication date=2015-11-24  Event code=EP/REG  Event code=FR/PLFP  Event indicator=Pos  Event type=Payment or non-payment notifications  Event type=Restitution or restoration  Reference to a national code Fee payment Derniere annuite payee   Annual fees payment date=2015-11-24     Year of payment of annual fees=7  Corresponding cc:  Designated or member state=FR     Event publication date=2016-11-17  Event code=EP/REG  Event code=FR/PLFP  Event indicator=Pos  Event type=Payment or non-payment notifications  Event type=Restitution or restoration  Reference to a national code Fee payment Derniere annuite payee   Annual fees payment date=2016-11-17     Year of payment of annual fees=8  Corresponding cc:  Designated or member state=FR     Event publication date=2017-11-20  Event code=EP/REG  Event code=FR/PLFP  Event indicator=Pos  Event type=Payment or non-payment notifications  Event type=Restitution or restoration  Reference to a national code Fee payment Derniere annuite payee   Annual fees payment date=2017-11-20     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=FR     Event publication date=2017-11-20  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-20     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=FR  MEMBER STATE LEGAL DETAILS FOR GB  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=GB     Event publication date=2015-09-16  Event code=EP/REG  Event code=GB/FG4D  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code European patent granted Corresponding cc:  Designated or member state=GB     Event publication date=2016-11-30  Event code=EP/REG  Event code=GB/732E  Event type=Administrative notifications  Event type=Reassignment  Reference to a national code Amendments to the register in respect of changes of name or changes affecting rights (sect. 32/1977) Corresponding cc:  Designated or member state=GB  REGISTERED BETWEEN 20161103 AND 20161109     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=GB  MEMBER STATE LEGAL DETAILS FOR GR  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=GR Corresponding appl: GR20150402517    Event publication date=2016-06-17  Event code=EP/REG  Event code=GR/EP  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Ep patent validated in greece Corresponding cc:  Designated or member state=GR   Effective date of the event=2016-02-01     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=GR  MEMBER STATE LEGAL DETAILS FOR HRP20151242  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=HR Corresponding appl: HRP20151242  Application date in the designated or member state=2015-11-18   Application number in the designated or member state=2015HR-0001242 Corresponding cc:  Designated or member state=HR Corresponding pat: HRP20151242  Publication stage code in the designated or member state=T1  Publication date in the designated or member state=2015-12-18   Publication number in the designated or member state=HRP20151242    Event publication date=2017-12-05  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-05     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=HR  MEMBER STATE LEGAL DETAILS FOR HUE028080  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=HU Corresponding appl: HUE09765114  Application date in the designated or member state=2009-12-09   Application number in the designated or member state=2009HU-E765114 Corresponding cc:  Designated or member state=HU Corresponding pat: HUE028080  Publication stage code in the designated or member state=T2  Publication date in the designated or member state=2016-11-28   Publication number in the designated or member state=HUE028080    Event publication date=2016-11-28  Event code=EP/REG  Event code=HU/AG4A  Event indicator=Pos  Event type=Examination events  Reference to a national code Filing of the translation of the text of european patents Eurpai szabadalmak szoevege forditasanak benyujtasa Corresponding cc:  Designated or member state=HU     Event publication date=2017-11-27  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-27     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=HU  MEMBER STATE LEGAL DETAILS FOR IE  Actual or expected expiration date=2016-09-21    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IE     Event publication date=2015-10-07  Event code=EP/REG  Event code=IE/FG4D  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code European patents granted designating ireland Corresponding cc:  Designated or member state=IE     Event publication date=2016-09-21  Event code=EP/REG  Event code=IE/MM4A  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Patent lapsed Corresponding cc:  Designated or member state=IE     Event publication date=2016-10-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=IE  MEMBER STATE LEGAL DETAILS FOR IS  Actual or expected expiration date=2016-04-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IS     Event publication date=2016-04-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=IS  MEMBER STATE LEGAL DETAILS FOR IT  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=IT     Event publication date=2017-12-19  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-19     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=IT  MEMBER STATE LEGAL DETAILS FOR LT  Actual or expected expiration date=2016-01-29    Legal state=DEAD    Status=REVOKED   Corresponding cc:  Designated or member state=LT     Event publication date=2016-01-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=LT     Event publication date=2016-02-10  Event code=EP/REG  Event code=LT/MG4D  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Invalidated european patent Europos patentai, laikomi ab initio negaliojanciais Corresponding cc:  Designated or member state=LT  MEMBER STATE LEGAL DETAILS FOR LU  Actual or expected expiration date=2016-07-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LU     Event publication date=2016-07-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=LU  MEMBER STATE LEGAL DETAILS FOR LV  Actual or expected expiration date=2016-01-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LV     Event publication date=2016-01-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=LV  MEMBER STATE LEGAL DETAILS FOR MC  Actual or expected expiration date=2016-07-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=MC     Event publication date=2016-07-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=MC  MEMBER STATE LEGAL DETAILS FOR MT  Actual or expected expiration date=2017-08-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=MT     Event publication date=2017-08-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=MT  MEMBER STATE LEGAL DETAILS FOR NL  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=NL     Event publication date=2016-02-03  Event code=EP/REG  Event code=NL/FP  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Reference to a national code Translation for ep filed (entry of ep into country) Description in original language not provided Corresponding cc:  Designated or member state=NL     Event publication date=2017-12-12  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-12     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=NL  MEMBER STATE LEGAL DETAILS FOR NO  Actual or expected expiration date=2016-01-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=NO     Event publication date=2016-01-29  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=NO  MEMBER STATE LEGAL DETAILS FOR PL  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=PL     Event publication date=2017-12-01  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-01     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=PL  MEMBER STATE LEGAL DETAILS FOR PT  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=PT     Event publication date=2015-12-01  Event code=EP/REG  Event code=PT/SC4A  Event indicator=Pos  Event type=Examination events  Reference to a national code Translation is available Corresponding cc:  Designated or member state=PT   Effective date of the event=2015-11-16  AVAILABILITY OF NATIONAL TRANSLATION     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=PT  MEMBER STATE LEGAL DETAILS FOR RO  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=RO     Event publication date=2017-11-16  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-16     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=RO  MEMBER STATE LEGAL DETAILS FOR SE  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=SE     Event publication date=2015-12-15  Event code=EP/REG  Event code=SE/TRGR  Event indicator=Pos  Event type=Event indicating In Force  Event type=Entry into national phase  Reference to a national code Translation of granted ep patent Europeiska patent som uppraetthalls i aendrad avfattning Corresponding cc:  Designated or member state=SE     Event publication date=2017-12-08  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-12-08     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=SE  MEMBER STATE LEGAL DETAILS FOR SI  Actual or expected expiration date=2016-11-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SI     Event publication date=2016-11-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=SI  MEMBER STATE LEGAL DETAILS FOR SK  Actual or expected expiration date=2029-12-09    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=SK Corresponding appl: SKE 19815    Event publication date=2016-04-01  Event code=EP/REG  Event code=SK/T3  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Translation of european patent specification into slovakian Spristupnene preklady europskych spisov Corresponding cc:  Designated or member state=SK     Event publication date=2017-11-28  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2017-11-28     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=SK  MEMBER STATE LEGAL DETAILS FOR SM  Actual or expected expiration date=2017-05-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SM     Event publication date=2017-05-31  Event code=EP/PG25  Event indicator=Ne(...)
专利类型码
A1B1
国别省市代码
若您需要申请原文,请登录。

最新评论

暂无评论。

登录后可以发表评论

意见反馈
返回顶部