Pesticidal indazole or benzotriazole derivatives 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP1171437 A1 2002-01-16 [EP1171437]EP1171437 B1 2003-10-08 [EP1171437] / 2002-01-162003-10-08
申请号/申请日
2000EP-0919009 / 2000-04-04
发明人
PILKINGTON BRIAN LESLIE;MATHEWS CHRISTOPHER JOHN;BARNETT SUSAN PATRICIA;SMITH STEPHEN CHRISTOPHER;BARNES NIGEL JOHN;WHITTINGHAM WILLIAM GUY;WILLIAMS JOHN;CLARKE ERIC DANIEL;WHITTLE ALAN JOHN;HUGHES DAVID JOHN;ARMSTRONG SARAH;VINER RU;
申请人
SYNGENTA;
主分类号
IPC分类号
A01N-043/56A01N-043/647A01N-043/80C07D-401/12C07D-405/12C07D-417/12
摘要
(EP1171437) A compound of formula (I) wherein G is either (i) or (ii), where M<1> or M<2> is bonded to A; n is 0 or 1; when G is (i), D is S, NR<7>, CR<8>=CR<9>, CR<8>=N, CR<8>=N(O), N=CR<9> or N(O)=CR<9>; when G is (ii), D is S or NR<7>; E is N, N-oxide or CR<10>; M<1> is OC(=Y), N(R<11>)C(=Y), N=C(OR<12>), N=C(SR<13>) or N=C(NR<14>R<15>) where O or N is the atom of attachment to the ring containing D and E; M<2> is N-C(=Y) where N is the atom of attachment to the ring containing D and E; Y is O, S or NR<16>; J is N or CR<17>; and A, R<1>, R<2>, R<3>, R<4>, R<5>, R<6>, R<7>, R<8>, R<9>, R<10>, R<11>, R<12>, R<13>, R<14> and R<15> are each certain organic or inorganic groups.  These compounds are useful in fungicidal, insecticidal, acaricidal, molluscicidal and hematicidal compositions.
机翻摘要
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地址
代理人
代理机构
;
优先权号
1999GB-0009062 1999-04-20 2000GB-0002039 2000-01-28 2000WO-GB01272 2000-04-04
主权利要求
(EP1171437)  1. A compound of formula (I): (see diagramm 1 page 111) wherein G is either (see diagramm 2 page 111) where M**1  or M**2  is bonded to A;  n is 0 or 1;  A is optionally substituted C1-6  alkylene, optionally substituted C2-6  alkenylene, optionally substituted C2-6  alkynylene, optionally substituted C1-6  alkylenoxy, optionally substituted oxy(C1-6 )alkylene, optionally substituted C1-6  alkylenethio, optionally substituted thio(C1-6 )alkylene, optionally substituted C1-6  alkylenamino, optionally substituted amino(C1-6 )alkylene, optionally substituted [C1-6  alkyleneoxy(C1-6 )alkylene], optionally substituted - [C1-6  alkylenethio(C1-6 )alkylene], optionally substituted [C1-6  alkylenesulfinyl(C1-6 )alkylene], optionally substituted [C1-6  alkylenesulfonyl(C1-6 )alkylene] or optionally substituted [C1-6  alkyleneamino(C1-6 )alkylene];  when G is (i), D is S, NR**7 , CR**8 =CR**9 , CR**8 =N, CR**8 =N(O), N=CR**9  or N(O)=CR**9 ;  when G is (ii), D is S or NR**7 ;  E is N, N-oxide or CR**10 ;  M**1  is OC(=Y), N(R**11 )C(=Y), N=C(OR**12 ), N=C(SR**13 ) or N=C(NR**14 R**15 ) where O or N is the atom of attachment to the ring containing D and E;  M**2  is N-C(=Y) where N is the atom of attachment to the ring containing D and E;  Y is O, S or NR**16 ;  J is N or CR**17 ;  R**1  is hydrogen, halogen, optionally substituted C1-6  alkyl, optionally substituted C2-6  alkenyl, optionally substituted C2-6  alkynyl, optionally substituted C1-6  alkoxy, optionally substituted C1-6  alkylthio, optionally  substituted C3-7  cycloalkyl, cyano, nitro or SF5 ;  R**2  is optionally substituted C1-10  alkyl, optionally substituted [C2-6  alkenyl(C1-6 )alkyl], optionally substituted [C2-6  alkynyl(C1-6 )alkyl], optionally substituted C3-7  cycloalkyl, optionally substituted C1-10  alkylcarbonyl, optionally substituted C1-10  alkoxycarbonyl, formyl, optionally substituted C1-10  alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, optionally substituted phenoxycarbonyl, optionally substituted C1-6  alkylthio, optionally substituted C1-6  alkylsulfinyl, optionally substituted C1-6  alkylsulfonyl, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl or R**18 R**19 NS;  R**3 , R**4  and R**5  are, independently, hydrogen, halogen, optionally substituted C1-6  alkyl, optionally substituted C1-6  alkoxy, optionally substituted C1-6  alkylthio, optionally substituted C1-6  alkylsulfinyl, optionally substituted C1-6  alkylsulfonyl, cyano, nitro, optionally substituted C1-6  alkylcarbonyl, optionally substituted C1-6  alkoxycarbonyl or SF5 ;  R**6  is hydrogen, cyano, optionally substituted C1-20  alkyl, optionally substituted C2-20  alkenyl(C1-6 )alkyl, optionally substituted C2-20  alkynyl(C1-6 )alkyl, optionally substituted C3-7  cycloalkyl, optionally substituted C5-6  cycloalkenyl, formyl, optionally substituted C1-20  alkoxycarbonyl, optionally substituted C1-20  alkylcarbonyl, aminocarbonyl, optionally substituted C1-20  alkylaminocarbonyl, optionally substituted di(C1-20 )alkylaminocarbonyl, optionally substituted aryloxycarbonyl, optionally substituted arylcarbonyl, optionally substituted arylaminocarbonyl, optionally substituted N-alkyl-N-arylaminocarbonyl, optionally substituted diarylaminocarbonyl, optionally substituted heteroaryloxycarbonyl, optionally substituted heteroarylcarbonyl, optionally substituted heteroarylaminocarbonyl, optionally substituted alkylheteroarylaminocarbonyl, optionally substituted diheteroarylaminocarbonyl, optionally substituted phenyl, optionally substituted heteroaryl, optionally substituted heterocyclyl, optionally substituted C1-20  alkylsulfonyl or optionally substituted arylsulfonyl;  R**7  is C1-6  alkyl;  R**8  and R**9  are, independently, hydrogen, halogen, cyano, nitro, optionally substituted C1-6  alkyl, optionally substituted C2-6  alkenyl, optionally substituted C2-6  alkynyl or optionally substituted C1-6  alkoxy;  R**10  is hydrogen, halogen, optionally substituted C1-6  alkyl,  optionally substituted C2-6  alkenyl, optionally substituted C2-6  alkynyl, optionally substituted C1-6  alkoxy, optionally substituted C1-6  alkylthio, optionally substituted - C1-6  alkylsulfinyl, optionally substituted C1-6  alkylsulfonyl, cyano, nitro, formyl, R**20 ON=C(R**21 ), optionally substituted C1-6  alkylcarbonyl, optionally substituted C1-6  alkoxycarbonyl or SF5 ;  or R**1  and R**10  together with the atoms to which they are attached may be joined to form a five, six or seven-membered saturated or unsaturated ring carbocylic or heterocyclic ring which may contain one or two hetero atoms selected from O, N and S and which may be optionally substituted by C1-6  alkyl, C1-6  haloalkyl or halogen;  R**11  is hydrogen, optionally substituted C1-10  alkyl, optionally substituted [C2-6  alkenyl(C1-6 )alkyl], optionally substituted [C2-6  alkynyl(C1-6 )alkyl], optionally substituted C3-7  cycloalkyl, optionally substituted C1-10  alkylcarbonyl, optionally substituted C1-10  alkoxycarbonyl, formyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, optionally substituted phenoxycarbonyl, optionally substituted C1-6  alkylthio, optionally substituted C1-6  alkylsulfinyl, optionally substituted C1-6  alkylsulfonyl, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl or R**22 R**23 NS;  R**12  is optionally substituted C1-10  alkyl, optionally substituted [C2-6  alkenyl(C1-6 )alkyl], optionally substituted [C2-6  alkynyl(C1-6 )alkyl], optionally substituted C3-7  cycloalkyl, optionally substituted C1-10  alkylcarbonyl, optionally substituted C1-10  alkoxycarbonyl, formyl, optionally substituted C1-10  alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, , amino, optionally substituted C1-6  alkylamino, optionally substituted di(C1-6 )alkylamino, optionally substituted phenoxycarbonyl, tri(C1-4 )alkylsilyl, aryldi(C1-4 )alkylsilyl, (C1-4 )alkyldiarylsilyl or triarylsilyl;  R**13  is optionally substituted C1-10  alkyl, optionally substituted [C2-6  alkenyl(C1-6 )alkyl], optionally substituted [C2-6  alkynyl(C1-6 )alkyl], optionally substituted C3-7  cycloalkyl, optionally substituted C1-10  alkylcarbonyl, optionally substituted C1-10  alkoxycarbonyl, optionally substituted C1-10  alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl or optionally substituted phenoxycarbonyl);  R**14  and R**15  are, independently optionally substituted C1-10  alkyl, optionally substituted C1-6  alkoxy, optionally substituted [C2-6  alkenyl(C1-6 )alkyl],  optionally substituted [C2-6  alkynyl(C1-6 )alkyl], optionally substituted C3-7  cycloalkyl, optionally substituted C1-10  alkylcarbonyl, optionally substituted C1-10  alkoxycarbonyl, formyl, optionally substituted C1-10 alkylaminocarbonyl, optionally substituted di(C1-10 )alkylaminocarbonyl, hydroxy, amino, optionally substituted C1-6  alkylamino, optionally substituted di(C1-6 )alkylamino, or optionally substituted phenoxycarbonyl;  R**16  is hydrogen, cyano, nitro, optionally substituted C1-6  alkyl, optionally substituted C3-7  cycloalkyl, optionally substituted (C2-6 )alkenyl(C1-6 )alkyl, optionally substituted (C2-6 )alkynyl(C1-6 )alkyl, optionally substituted phenyl, optionally substituted heteroaryl, optionally substituted C1-6  alkylcarbonyl, optionally substituted C1-6  alkoxycarbonyl, optionally substituted C1-6  alkylamino, optionally substituted di(C1-6 )alkylamino, optionally substituted C1-6  alkylcarbonylamino, optionally substituted C1-6  alkoxycarbonylamino, optionally substituted C1-6  alkoxy, optionally substituted C1-6  alkylthio, optionally substituted C1-6  alkylsulfinyl, optionally substituted C1-6  alkylsulfonyl, optionally substituted arylthio, optionally substituted arylsulfinyl, optionally substituted arylsulfonyl or C1-6  acyloxy;  R**17  is hydrogen, halogen, nitro, cyano, optionally substituted C1-8  alkyl, optionally substituted C2-6  alkenyl, optionally substituted C2-6  alkynyl, optionally substituted C3-7  cycloalkyl, optionally substituted C1-6  alkoxycarbonyl, optionally substituted C1-6  alkylcarbonyl, optionally substituted C1-6  alkylaminocarbonyl, optionally substituted di(C1-6 )alkylaminocarbonyl, optionally substituted phenyl or optionally substituted heteroaryl;  R**18  and R**19  are, independently, optionally substituted C1-6  alkyl or R**18  and R**19  together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6  alkyl groups;  R**20  is hydrogen, optionally substituted phenyl, optionally substituted phenyl(C1-4 )alkyl or optionally substituted C1-20  alkyl;  R**21  is hydrogen, optionally substituted phenyl or optionally substituted C1-6  alkyl;  and R**22  and R**23  are, independently, optionally substituted C1-6  alkyl or R**22  and R**23  together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6  alkyl groups;   wherein the optional substituents, when present, on the alkylene, alkenylene or alkynylene moieties are, subject to valency constraints, one or more of halogen, C1-6  alkyl, C1-6  haloalkyl, C1-6  cyanoalkyl, C1-6  alkoxy(C1-6 ) alkyl, C1-6  alkoxy, cyano, =O, =NR**24  and =CR**25 R**26 , wherein R**24  is C1-6  alkyl, C1-6  haloalkyl, OR**27  or R**28 R**29 N;  where R**25  and R**26  are, independently, hydrogen, C1-6  alkyl, C1-6  alkoxy, C1-6  haloalkyl, cyano, C1-6  alkoxycarbonyl, C1-6  alkylcarbonyl or R**30 R**31 N;  R**27  is C1-6  alkyl, C1-6  haloalkyl or phenyl(C1-2 )alkyl;  R**28  and R**29  are, independently, hydrogen, C1-8  alkyl, C3-7  cycloalkyl, C2-6  alkenyl(C1-6 )alkyl, C2-6  alkynyl(C1-6 )alkyl, C2-6  haloalkyl, C1-6  alkoxy(C1-6 )alkyl, C1-6  alkoxycarbonyl(C1-6 )alkyl, carboxy(C1-6 )alkyl or phenyl(C1-2 )alkyl or R**28  and R**29  together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6  alkyl groups;  R**30  and R**31  are, independently, hydrogen, C1-8  alkyl, C3-7  cycloalkyl, C2-6  alkenyl(C1-6 )alkyl, C2-6  alkynyl(C1-6 )alkyl, C2-6  haloalkyl, C1-6  alkoxy-(C1-6 )alkyl, C1-6  alkoxycarbonyl(C1-6 )alkyl, carboxy(C1-6 )alkyl or phenyl(C1-2 )alkyl;  or R**30  and R**31  together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selectedfrom O, N or S and which may be optionally substituted by one or two C1-6  alkyl groups;  and wherein each alkyl moiety is a straight or branched chain and, when present, the optional substituents on alkyl are one or more of halogen, nitro, cyano, HO2 C, C1-10  alkoxy (itself optionally substituted by C1-10  alkoxy), aryl-(C1-4 )alkoxy, C1-10  alkylthio, C1-10  alkylcarbonyl, C1-10  alkoxycarbonyl, C1-6  alkylaminocarbonyl, di(C1-6  alkyl)aminocarbonyl, (C1-6 )alkylcarbonyloxy, optionally substituted phenyl, heteroaryl, aryloxy, arylcarbonyloxy, heteroaryloxy, heterocyclyl, heterocyclyloxy, C3-7  cycloalkyl (itself optionally substituted with (C1-6 )alkyl or halogen), C3-7  cycloalkyloxy, C5-7  cycloalkenyl, C1-6  alkylsulfonyl, C1-6  alkylsulfinyl, tri(C1-4 )alkylsilyl, tri(C1-4 )alkylsilyl-(C1-6 )alkoxy, aryldi(C1-4 )alkylsilyl, (C1-4 )alkyldiarylsilyl, triarylsilyl, =N-OR' and =N-NR'R";  where R' and R" are, independently, C1-6  alkyl or C1-6  haloalkyl;  and where the alkenyl and alkynyl moieties are in the form of straight or branched chains, and the alkenyl moieties, where appropriate, can be of either the (E)- or (Z)-configuration;  and, when present, the optional substituents on alkenyl or alkynyl are one or more of halogen, aryl and C3-7   cycloalkyl;  and wherein acyl is optionally substituted C1-6  alkylcarbonyl, optionally substituted C2-6  alkenylcarbonyl, optionally substituted C2-6  alkynylcarbonyl, optionally substituted arylcarbonyl or optionally substituted heteroarylcarbonyl;  and wherein halogen is fluorine, chlorine, bromine or iodine;  haloalkyl groups are alkyl groups which are optionally substituted with one or more of the same or different halogen atoms;  aryl is phenyl, naphthyl, anthracyl, fluorenyl and indenyl;  heteroaryl is an aromatic ring containing up to 10 atoms including one or more heteroatoms selected from O, S and N;  heterocycle and heterocyclyl are a non-aromatic ring containing up to 10 atoms including one or more heteroatoms selected from O, S and N;  cycloalkyl is cyclopropyl, cyclopentyl and cyclohexyl and the optional substituents for cycloalkyl are halogen, cyano and C1-3  alkyl;  cycloalkenyl is cyclopentenyl and cyclohexenyl and the optional substituents for cycloalkenyl are C1-3  alkyl, halogen and cyano;  carbocyclic rings are aryl, cycloalkyl and cycloalkenyl groups;  and for substituted phenyl moieties, heterocyclyl and heteroaryl groups the substituents are independently selected from one or more of halogen, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy(C1-6 )alkyl, C1-6  alkoxy, C1-6  haloalkoxy, C1-6  alkylthio, C1-6  haloalkylthio, C1-6  alkylsulfinyl, C1-6  haloalkylsulfinyl, C1-6  alkylsulfonyl, C1-6  haloalkylsulfonyl, C2-6  alkenyl, C2-6  haloalkenyl, C2-6  alkynyl, C3-7  cycloalkyl, nitro, cyano, CO2 H, C1-6  alkylcarbonyl, C1-6  alkoxycarbonyl, R**32 R**33 N or R**34 R**35 NC(O) wherein R**32 , R**33 , R**34  and R**35  are, independently, hydrogen or C1-6  alkyl;  and wherein dialkylamino substituents include those where the dialkyl groups together with the N atom to which they are attached form a five, six or seven-membered heterocyclic ring which may contain one or two further hetero atoms selected from O, N or S and which may be optionally substituted by one or two C1-6  alkyl groups;  and when heterocyclic rings are formed by joining two groups on an N atom, the resulting rings are pyrrolidine, piperidine, thiomorpholine and morpholine each of which may be substituted by one or two (C1-6 )alkyl groups.   2. A compound as claimed in claim 1 of formula (IA): (see diagramm 1 page 117) wherein A, G, J, R**3 , R**4 , R**5  and R**6  are as claimed in claim 1.  3. A compound of formula (I) as claimed in claim 1 or a compound of formula (IA) as claimed in claim 2 wherein, when G is (i) as defined in claim 1, D is S or CR**8 =CR**9 , where R**8  and R**9  are, independently, hydrogen, halogen, C1-6  alkyl, C1-6  haloalkyl C2-6  alkenyl, C2-6  alkynyl, C1-6  alkoxy or C1-6  haloalkoxy;  when G is (ii) as defined in claim 1, D is S;  E is N or CR**10  where R**10  is hydrogen, halogen, C1-6  alkyl, C1-6  haloalkyl, - C1-6  alkoxy, C1-6  haloalkoxy, C1-6  alkoxy (C1-6 )alkyl, C1-6  alkylthio or SF5 ;  or R**1  and R**10  together with the atoms to which they are attached form a benzene ring optionally substituted by C1-6  alkyl, C1-6  haloalkyl or halogen;  and M**1  is N(R**11 )C(=O) where R**11  is hydrogen, C1-6  alkyl, C1-6  alkoxy(C1-6 )alkyl, benzyloxymethyl or benzoyloxymethyl.  4. A compound of formula (I) as claimed in claim 1 or 3 or a compound of formula (IA) as claimed in claim 2 or 3 wherein A is C1-4  alkylene, -C(O)- or C1-4  alkyleneoxy.  5. A compound of formula (I) as claimed in claim 1, 3 or 4 or a compound of formula (IA) as claimed in claim 2, 3 or 4 wherein G is (i) as defined in claim 1 and n is 0.  6. A compound of formula (I) as claimed in claim 1, 3, 4 or 5 or a compound of formula (IA) as claimed in claim 2, 3, 4 or 5 wherein R**3 , R**4  and R**5  are, independently, hydrogen, C1-3  alkyl or halogen.   7. A compound of formula (I) as claimed in claim 1, 3, 4, 5 or 6 or a compound of formula (IA) as claimed in claim 2, 3, 4, 5 or 6 wherein R**6  is C1-10  alkyl or C1-10  haloalkyl (each one of which may be substituted with a C1-6  alkyloxime, C1-6  haloalkyloxime, C1-6  alkylhydrazone or C1-6  haloalkylhydrazone group) or C1-6  cyanoalkyl, C2-6  alkenyl(C1-6 )alkyl, C2-6  alkynyl(C1-6 )alkyl, C3-7  cycloalkyl, C3-7  halocycloalkyl, C3-7  cyanocycloalkyl, C1-3  alkyl(C3-7 )cycloalkyl, C1-3  alkyl(C3-7 )halocycloalkyl, C5-6  cycloalkenyl, C3-7  cycloalkyl(C1-6 )alkyl, C5-6  cycloalkenyl(C1-6 )alkyl, C2-6  haloalkenyl(C1-6 )alkyl, C1-6  cyanoalkenyl(C1-6 )alkyl, C1-6  alkoxy(C1-6 )alkyl, C3-6  alkenyloxy(C1-6 )alkyl, C3-6  alkynyloxy(C1-6 )alkyl, aryloxy(C1-6 )alkyl, C1-6  carboxyalkyl, C1-6  alkylcarbonyl(C1-6 )alkyl, C2-6  alkenylcarbonyl(C1-6 )alkyl, C2-6  alkynylcarbonyl(C1-6 )alkyl, C1-6  alkoxycarbonyl(C1-6 )alkyl, C3-6  alkenyloxycarbonyl(C1-6 )alkyl, C3-6  alkynyloxycarbonyl(C1-6 )alkyl, aryloxycarbonyl(C1-6 )alkyl, C1-6  alkylthio(C1-6 )alkyl, C1-6  alkylsulfinyl(C1-6 )alkyl, C1-6  alkylsulfonyl(C1-6 )alkyl, aminocarbonyl(C1-6 )alkyl, aminocarbonyl(C2-6 )alkenyl, aminocarbonyl(C2-6 )alkynyl, C1-6 alkylaminocarbonyl(C1-6 )alkyl, di(C1-6 )alkylaminocarbonyl(C1-6 )alkyl, C1-6 alkylaminocarbonyl(C2-6 )alkenyl(C1-6 )alkyl, di(C1-6 )alkylaminocarbonyl(C2-6 )alkenyl(C1-6 )alkyl, alkylaminocarbonyl(C2-6 )alkynyl(C1-6 )alkyl, di(C1-6 )alkylaminocarbonyl(C2-6 )alkynyl(C1-6 )alkyl, phenyl (optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy or C1-6  haloalkoxy), phenyl(C1-4 )alkyl (wherein the phenyl group is optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy or C1-6  haloalkoxy), phenyl(C2-4 )alkenyl(C1-6 )alkyl, (wherein the phenyl group is optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy, C1-6  alkylsulfonyl or C1-6  haloalkoxy), heteroaryl (optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy or C1-6  haloalkoxy), heterocyclyl (wherein the heterocyclyl group is optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy or C1-6  haloalkoxy), heteroaryl(C1-4 )alkyl (wherein the heteroaryl group is optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy, C1-6  alkylsulfonyl or C1-6  haloalkoxy)or heterocyclyl(C1-4 )alkyl (wherein the heterocyclyl  group is optionally substituted by halo, nitro, cyano, C1-6  alkyl, C1-6  haloalkyl, C1-6  alkoxy or C1-6  haloalkoxy).  8. A compound of formula (I) as claimed in claim 1, 3, 4, 5, 6 or 7 or a compound of formula (IA) as claimed in claim 2, 3, 4, 5, 6 or 7 wherein J is N or CR**17  where R**17  is hydrogen, C1-6  alkyl, C1-6  haloalkyl, cyano, halogen or nitro.  9. A process for preparing a compound of formula (I) as claimed in claim 1 comprising   (a) where Y is oxygen, reacting a compound of formula (II) (see diagramm 1 page 119) where D, E, R**1  and R**11  are as defined in claim 1 with a compound of formula (III) (see diagramm 2 page 119) where Y is oxygen, X**1  is a leaving group and A, J, R**3 , R**4 , R**5  and R**6  are as defined in claim 1;  or  (b) where Y is sulphur, preparing a compound of formula (I) as claimed in claim 1 where Y is oxygen using the method described in (a) and then reacting this compound with a thionating agent.   10. A fungicidal, insecticidal, acaricidal, molluscicidal or nematicidal composition comprising a fungicidally, insecticidally, acaricidally, molluscicidally or nematicidally effective amount of a compound of formula (I) as claimed in claim 1 and a carrier or diluent therefor.   11. A method of combating and controlling fungi comprising applying to a plant, to a seed of a plant, to the locus of the plant or seed or to the soil a fungicidally effective amount of either a compound of formula (I) as claimed in claim 1.  12. A method of combating and controlling insects, acarines, nematodes or molluscs which comprises applying to a pest, to a locus of a pest, or to a plant susceptible to attack by a pest an insecticidally, acaricidally, nematicidally or molluscicidally effective amount of a compound of formula (I) as claimed in claim 1.
法律状态
(EP1171437) LEGAL DETAILS FOR EP1171437  Actual or expected expiration date=2011-07-14    Legal state=DEAD    Status=LAPSED     Event publication date=2000-04-04  Event code=EP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=EP EP00919009  Application date=2000-04-04  Standardized application number=2000EP-0919009     Event publication date=2002-01-16  Event code=EP/A1  Event type=Examination events  Application published with search report  Publication country=EP  Publication number=EP1171437  Publication stage Code=A1  Publication date=2002-01-16  Standardized publication number=EP1171437     Event publication date=2002-01-16  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE    Event publication date=2002-01-16  Event code=EP/17P  Event indicator=Pos  Event type=Examination events  Request for examination filed Pruefungsantrag gestellt  Effective date of the event=2001-11-20     Event publication date=2002-01-16  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 AL PAYMENT 20011120 LT PAYMENT 20011120 LV PAYMENT 20011120 MK PAYMENT 20011120 RO SI PAYMENT 20011120     Event publication date=2002-03-20  Event code=EP/17Q  Event indicator=Pos  Event type=Examination events  First examination report Erster pruefungsbescheid  Effective date of the event=2002-02-04     Event publication date=2002-09-18  Event code=EP/RAP1  Event type=Change of name or address  Event type=Reassignment  Transfer of rights of an application Anmelder uebertragung (korr.)    Event publication date=2003-10-08  Event code=EP/B1  Event indicator=Pos  Event type=Event indicating In Force  Patent specification  Publication country=EP  Publication number=EP1171437  Publication stage Code=B1  Publication date=2003-10-08  Standardized publication number=EP1171437     Event publication date=2003-10-08  Event code=EP/AK  Event indicator=Pos  Event type=Designated states  Designated contracting states: Benannte vertragsstaaten AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE    Event publication date=2003-10-08  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 AL LT LV MK SI    Event publication date=2004-09-29  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=2004-07-09     Event publication date=2011-07-14  Event code=EP/LAPS  Event indicator=Neg  Event type=Event indicating Not In Force  Lapse of the protection rights for all corresponding member states EP lapsed due to lapse of contracting member states AT BE CH CY DE DK ES FI FR GB GR IE IT LI LU MC NL PT SE     Event publication date=2011-07-14  Event code=EP/EXSN  Notification: EP extension states status not included in change to EP status MEMBER STATE LEGAL DETAILS FOR AT251621  Actual or expected expiration date=2010-04-04    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=AT Corresponding appl: AT00919009  Application date in the designated or member state=2000-04-04   Application number in the designated or member state=2000AT-0919009T Corresponding cc:  Designated or member state=AT Corresponding pat: AT251621  Publication stage code in the designated or member state=T  Publication date in the designated or member state=2003-10-15   Publication number in the designated or member state=ATE251621    Event publication date=2009-04-15  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=2009-04-15     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=AT     Event publication date=2010-04-04  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 Corresponding cc:  Designated or member state=AT   Effective date of the event=2010-04-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR BE  Actual or expected expiration date=2010-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=BE     Event publication date=2009-04-28  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=2009-04-28     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=BE     Event publication date=2010-04-30  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 Corresponding cc:  Designated or member state=BE   Effective date of the event=2010-04-30  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2010-10-31  Event code=EP/BERE  Event indicator=Neg  Event type=Event indicating Not In Force  BE: Lapsed BE: Dechu Corresponding cc:  Designated or member state=BE   Effective date of the event=2010-04-30  MEMBER STATE LEGAL DETAILS FOR CH  Actual or expected expiration date=2010-04-30    Legal state=DEAD    Status=EXPIRED   Corresponding cc:  Designated or member state=CH     Event publication date=2003-10-15  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=2004-04-30  Event code=EP/REG  Event code=CH/PFA  Event type=Change of name or address  Event type=Reassignment  Reference to a national code Name/firm changed Namens-/firmenaenderung Corresponding cc:  Designated or member state=CH  SYNGENTA LIMITED#EUROPEAN REGIONAL CENTRE PRIESTLEY ROAD SURREY RESEARCH PARK#GUILDFORD SURREY GU2 7YH (GB) -TRANSFER TO- SYNGENTA LIMITED SYNGENTA EUROPEAN REGIONAL CENTRE#PRIESTLEY ROAD, SURREY RESEARCH PARK,#GUILDFORD, SURREY GU2 7YH (GB)     Event publication date=2009-04-16  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=2009-04-16     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=CH     Event publication date=2010-04-30  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 Corresponding cc:  Designated or member state=CH   Effective date of the event=2010-04-30  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2010-11-30  Event code=EP/REG  Event code=CH/PL  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Patent ceased Loeschung/radiation/radiazion Corresponding cc:  Designated or member state=CH  MEMBER STATE LEGAL DETAILS FOR CY  Actual or expected expiration date=2003-10-08    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CY     Event publication date=2003-10-08  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 Corresponding cc:  Designated or member state=CY   Effective date of the event=2003-10-08  LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  MEMBER STATE LEGAL DETAILS FOR DE60005808  Actual or expected expiration date=2010-11-03    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=DE Corresponding appl: DE60005808  Application date in the designated or member state=2000-04-04   Application number in the designated or member state=2000DE-6005808 Corresponding cc:  Designated or member state=DE Corresponding pat: DE60005808  Publication stage code in the designated or member state=D1  Publication date in the designated or member state=2003-11-13   Publication number in the designated or member state=DE60005808    Event publication date=2003-11-13  Event code=EP/REF  Event type=Entry into national phase  Corresponds to: Corresponding cc:  Designated or member state=DE     Event publication date=2009-04-02  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=2009-04-02     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=DE     Event publication date=2010-11-03  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 Corresponding cc:  Designated or member state=DE   Effective date of the event=2010-11-03  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR DK1171437  Actual or expected expiration date=2010-05-03    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=DK Corresponding appl: DK00919009  Application date in the designated or member state=2000-04-04   Application number in the designated or member state=2000DK-0919009 Corresponding cc:  Designated or member state=DK Corresponding pat: DK1171437  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2004-02-02   Publication number in the designated or member state=DK1171437T    Event publication date=2004-02-02  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     Event publication date=2009-04-15  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=2009-04-15     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=DK     Event publication date=2010-05-03  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 Corresponding cc:  Designated or member state=DK   Effective date of the event=2010-05-03  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2010-12-13  Event code=EP/REG  Event code=DK/EBP  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Patent lapsed Ep patentet bortfaldet Corresponding cc:  Designated or member state=DK  MEMBER STATE LEGAL DETAILS FOR ES2208303  Actual or expected expiration date=2011-07-14    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=ES Corresponding appl: ES00919009  Application date in the designated or member state=2000-04-04   Application number in the designated or member state=2000ES-0919009T Corresponding cc:  Designated or member state=ES Corresponding pat: ES2208303  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2004-06-16   Publication number in the designated or member state=ES2208303    Event publication date=2004-06-16  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     Event publication date=2009-05-08  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=2009-05-08     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=ES     Event publication date=2010-04-05  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 Corresponding cc:  Designated or member state=ES   Effective date of the event=2010-04-05  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2011-07-04  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 Corresponding cc:  Designated or member state=ES   Effective date of the event=2011-07-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2011-07-14  Event code=EP/REG  Event code=ES/FD2A  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Announcement of lapse in spain Ep-patente caducidades Corresponding cc:  Designated or member state=ES   Effective date of the event=2011-07-14  MEMBER STATE LEGAL DETAILS FOR FI  Actual or expected expiration date=2010-04-04    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=FI     Event publication date=2009-04-16  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=2009-04-16     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=FI     Event publication date=2010-04-04  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 Corresponding cc:  Designated or member state=FI   Effective date of the event=2010-04-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR FR  Actual or expected expiration date=2010-12-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=FR     Event publication date=2004-07-23  Event code=EP/ET  Event indicator=Pos  Event type=Event indicating In Force  FR: Translation filed FR: Traduction a ete remise Corresponding cc:  Designated or member state=FR     Event publication date=2009-04-17  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=2009-04-17     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=FR     Event publication date=2010-04-30  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 Corresponding cc:  Designated or member state=FR   Effective date of the event=2010-04-30  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2010-12-30  Event code=EP/REG  Event code=FR/ST  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Reference to a national code Notification of lapse Constatation de decheances Corresponding cc:  Designated or member state=FR   Effective date of the event=2010-12-30  MEMBER STATE LEGAL DETAILS FOR GB  Actual or expected expiration date=2010-04-04    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=GB     Event publication date=2003-10-08  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=2009-04-01  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=2009-04-01     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=GB     Event publication date=2010-04-04  Event code=EP/GBPC  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  GB: European patent ceased through non-payment of renewal fee Corresponding cc:  Designated or member state=GB   Effective date of the event=2010-04-04     Event publication date=2010-04-04  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 Corresponding cc:  Designated or member state=GB   Effective date of the event=2010-04-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR GR  Actual or expected expiration date=2004-01-08    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=GR     Event publication date=2004-01-08  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 Corresponding cc:  Designated or member state=GR   Effective date of the event=2004-01-08  LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  MEMBER STATE LEGAL DETAILS FOR IE  Actual or expected expiration date=2010-04-05    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IE     Event publication date=2003-11-12  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=2009-04-20  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=2009-04-20     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=IE     Event publication date=2010-04-05  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 Corresponding cc:  Designated or member state=IE   Effective date of the event=2010-04-05  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2011-01-19  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  MEMBER STATE LEGAL DETAILS FOR IT  Actual or expected expiration date=2010-04-04    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IT     Event publication date=2009-04-23  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=2009-04-23     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=IT     Event publication date=2010-04-04  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 Corresponding cc:  Designated or member state=IT   Effective date of the event=2010-04-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR LI  Actual or expected expiration date=2010-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LI     Event publication date=2010-04-30  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 Corresponding cc:  Designated or member state=LI   Effective date of the event=2010-04-30  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR LT  Actual or expected expiration date=2003-10-08    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LT     Event publication date=2004-03-25  Event code=EP/LTIE  Event indicator=Neg  Event type=Event indicating Not In Force  LT: Invalidation of european patent or patent extension LT: Invalidation of european patent extension Corresponding cc:  Designated or member state=LT   Effective date of the event=2003-10-08  MEMBER STATE LEGAL DETAILS FOR LU  Actual or expected expiration date=2010-04-04    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LU     Event publication date=2009-04-24  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=2009-04-24     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=LU     Event publication date=2010-04-04  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 Corresponding cc:  Designated or member state=LU   Effective date of the event=2010-04-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR MC  Actual or expected expiration date=2004-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=MC     Event publication date=2004-04-30  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 Corresponding cc:  Designated or member state=MC   Effective date of the event=2004-04-30  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR NL  Actual or expected expiration date=2010-11-01    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=NL     Event publication date=2009-04-05  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=2009-04-05     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=NL     Event publication date=2010-11-01  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 Corresponding cc:  Designated or member state=NL   Effective date of the event=2010-11-01  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2010-11-10  Event code=EP/REG  Event code=NL/V1  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Lapsed because of non-payment of the annual fee Vervallen wegens niet betalen van een jaarcijns Corresponding cc:  Designated or member state=NL   Effective date of the event=2010-11-01  MEMBER STATE LEGAL DETAILS FOR PT  Actual or expected expiration date=2010-10-04    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=PT     Event publication date=2004-03-31  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=2004-01-08  AVAILABILITY OF NATIONAL TRANSLATION     Event publication date=2009-03-30  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=2009-03-30     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=PT     Event publication date=2010-10-04  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 Corresponding cc:  Designated or member state=PT   Effective date of the event=2010-10-04  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  MEMBER STATE LEGAL DETAILS FOR SE  Actual or expected expiration date=2010-04-05    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SE     Event publication date=2004-01-07  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=2009-04-07  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=2009-04-07     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=SE     Event publication date=2010-04-05  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 Corresponding cc:  Designated or member state=SE   Effective date of the event=2010-04-05  LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES     Event publication date=2010-11-30  Event code=EP/EUG  Event indicator=Neg  Event type=Event indicating Not In Force  SE: European patent has lapsed SE: Europeiskt patent har upphoert att gaella Corresponding cc:  Designated or member state=SE
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