Isoxazoline-substituted benzamide compound and harmful organism-controlling agent 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP1932836 A1 2008-06-18 [EP1932836]EP1932836 A4 2009-11-04 [EP1932836]EP1932836 B1 2013-11-06 [EP1932836] / 2008-06-182009-11-042013-11-06
申请号/申请日
2006EP-0797653 / 2006-09-01
发明人
MITA TAKESHI;FURUKAWA YUKI;TOYAMA KEN-ICHI;YAOSAKA MANABU;IKEDA EITATSU;MASUZAWA YOSHIHIDE;KOMODA MITSUAKI;
申请人
NISSAN CHEMICAL INDUSTRIES;
主分类号
IPC分类号
A01N-043/80A01P-007/02A01P-007/04C07D-261/04C07D-413/04
摘要
(EP1932836) An isoxazoline-substituted benzamide compound of formula (1) or a salt thereof: wherein A 1 , A 2 and A 3 independently of one another are carbon atom or nitrogen atom, G is benzene ring, etc., W is oxygen atom or sulfur atom, etc., X is halogen atom, C 1 -C 6 haloalkyl, etc., Y ia halogen atm, C 1 -C 6 alkyl, etc., R 1 is -CH=NOR 1a , -C(O)OR 1c , -C(O)NHR 1d , phenyl substituted with (Z) p1 , D-14, D-52, D-53, D-55 to D-59, etc., R 1a is C 1 -C 6 alkyl, etc., R 1c is C 1 -C 6 alkyl, etc., R 1d is hydrogen atom, -C(O)R 15 , -C(O)OR 15 , etc., R 2 is C 1 -C 6 alkyl, -CH 2 R 14a , C 1 -C 6 alkynyl, -C(O)R 15 , -C(O)OR 15 , etc., further when R 1 is -CH=NOR 1a , -C(O)OR 1c or -C(O)N(R 1e )R 1d , R 2 may be hydrogen atom, R 3 is C 1 -C 6 haloalkyl, etc., R 14a is cyano, -OR 25 , etc., R 15 is C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 4 alkoxy C 1 -C 4 alkyl, C 1 -C 4 alkylthio C 1 -C 4 alkyl, C 3 -C 6 cycloalkyl, C 2 -C 6 alkenyl, etc., R 25 is C 1 -C 4 alkyl, C 1 -C 4 haloalkyl, -C(O)R 32 or -C(O)OR 32 , etc., R 32 is C 1 -C 6 alkyl or C 3 -C 6 cycloalkyl, etc., Z is halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 alkoxy, etc., m is an integer of 0 to 5, n is an integer of 0 to 4, p1 is an interger of 1 to 5.  The pesticide containing these compounds.
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
2005JP-0254446 2005-09-02 2005JP-0254449 2005-09-02 2005JP-0254451 2005-09-02 2005JP-0257344 2005-09-06 2006JP-0045804 2006-02-22 2006JP-0085597 2006-03-27 2006JP-0113060 2006-04-17 2006JP-0139953 2006-05-19 2006WO-JP317797 2006-09-01
主权利要求
(EP1932836)  1. An isoxazoline-substituted benzamide compound of formula (1) or a salt thereof: (see diagramm) wherein A **1, A **2and A **3 independently of one another are carbon atom or nitrogen atom, G is benzene ring, nitrogen-containing 6-membered aromatic heterocyclic ring, furan ring, thiophene ring, or 5-membered aromatic heterocyclic ring containing two or more hetero atoms selected from oxygen atom, sulfur atom and nitrogen atom,  W is oxygen atom or sulfur atom,  X is halogen atom, cyano, nitro, azido, -SCN, -SF 5, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **4, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with R **4, E-1 to E-50, C 2-C 6alkenyl, C 2-C 6alkenyl arbitrarily substituted with R **4, C 3-C 8cycloalkenyl, C 3-C 8halocycloalkenyl, C 2-C 6alkynyl, C 2-C 6alkynyl arbitrarily substituted with R **4, -OH, -OR **5, -OSO 2R **5, -SH, -S(O) rR **5, -NH 2, -N(R **7)R **6, -N=CHOR **8, -N=C(R **9)OR **8, -CHO, -C(O)R **9, -C(O)OR **9, -C(O)SR **9, -C(O)NH 2, -C(O)N(R **10)R **9, -C(S)OR **9, -C(S)SR **9, -C(S)NH 2, -C(S)N(R **10)R **9, -CH=NOR **11, -C(R **9)=NOR **11, M-5, M-20, M-40 to M-43, M-46 to M-48, -S(O) 2OR **9, -S(O) 2NH 2,  -S(O) 2N(R **10)R **9, -Si(R **12a)(R **12b)R **12, phenyl, phenyl substituted with (Z) P1, or D-1 to D-65, when m is an integer of 2 or more, each X may be identical with or different from each other,  further, when two Xs are adjacent, the adjacent two Xs may form 5-membered or 6-membered ring together with carbon atoms to which the two Xs are bonded by forming -CH 2CH 2CH 2-, -CH 2CH 2O-, -CH 2OCH 2-, -OCH 2O-, -CH 2CH 2S-, -CH 2SCH 2-, -CH 2CH 2N(R **13)-, -CH 2N(R **13)CH 2-, -CH 2CH 2CH 2CH 2-, -CH 2CH 2CH 2O-, -CH 2CH 2OCH 2-, -CH 2OCH 2O-, -OCH 2CH 2O-, -OCH 2CH 2S-, -CH 2CH=CH-, -OCH=CH-, -SCH=CH-, -N(R **13)CH=CH-, -OCH=N-, -SCH=N-, -N(R **13)CH=N-, -N(R **13)N=CH-, -CH=CHCH=CH-, -OCH 2CH=CH-, -N=CHCH=CH-, -N=CHCH=N- or -N=CHN=CH-, in this case, hydrogen atoms bonded to each carbon atom forming the ring may be arbitrarily substituted with Z, further when the hydrogen atoms are substituted with two or more Zs at the same time, each Z may be identical with or different from each other,  Y is halogen atom, cyano, nitro, azido, -SCN, -SF 5, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **4, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with R **4, E-1 to E-50, C 2-C 6alkynyl, C 2-C 6alkynyl arbitrarily substituted with R **4, -OH, -OR **5, -OSO 2R **5, -SH, -S(O) rR **5, -NH 2, -N(R **7)R **6, -N(R **7)C(O)R **9a, -N(R **7)C(O)OR **9a, -N(R **7)C(O)SR **9a, -N(R **7)C(S)OR **9a, -N(R **7)C(S)SR **9a, -N(R **7)S(O) 2R **9a, -N=CHOR **8, -N=C(R **9)OR **8, -C(O)NH 2, -C(O)N(R **10)R **9, -C(S)NH 2, -C(S)N(R **10)R **9, -Si(R **12a)(R **12b)R **12, phenyl, phenyl substituted with (Z) p1, D-1 to D-65, when n is an integer of 2 or more, each Y may be identical with or different from each other,  further, when two Ys are adjacent, the adjacent two Ys may form 5-membered or 6-membered ring together with carbon atoms to which the two Ys are bonded by forming -CH 2CH 2CH 2-, -CH 2CH 2O-, -CH 2OCH 2-, -OCH 2O-, -CH 2CH 2S-, -CH 2SCH 2-, -SCH 2S-, -CH 2CH 2CH 2CH 2-, -CH 2CH 2CH 2O-, -CH 2CH 2OCH 2-, -CH 2OCH 2O-, -OCH 2CH 2O-, -OCH 2CH 2S-, -SCH 2CH 2S-, -OCH=N- or -SCH=N-, in this case, hydrogen atoms bonded to each carbon atom forming the ring may be arbitrarily substituted with Z, further when the hydrogen atoms are substituted with two or more Zs at the same time, each Z may be identical with or different from each other, R **1 is -C(R **1b)=NOR **1a, M-5, M-20, M-48, -C(O)OR **1c, -C(O)SR **1c, -C(S)OR **1c, -C(S)SR **1c, -C(O)N(R **1e)R **1d, -C(S)N(R **1e)R **1d, -C(R **1b)=NN(R **1e)R **1f, phenyl, phenyl substituted with (Z) p1 or D-1 to D-65,  R **1a is hydrogen atom, C 1-C 12alkyl, C 1-C 12haloalkyl, C 1-C 6alkyl arbitrarily substituted with R **14, C 3-C 12cycloalkyl, C 3-C 12halocycloalkyl, C 3-C 8cyloalkyl arbitrarily substituted with R **14, E-4 to E-10, E-24 to E-29, E-31, E-32, E-35, E-46, C 3-C 12alkenyl, C 3-C 12haloalkenyl, C 3-C 6alkenyl arbitrarily substituted with R **14, C 3-C 12cycloalkenyl, C 3-C 12halocycloalkenyl, C 3-C 12alkynyl, C 3-C 12haloalkynyl, C 3-C 6alkynyl arbitrarily substituted with R **14, phenyl, phenyl substituted with (Z) p1, D-52, D-55 to D-58 or D-59, R **1b is hydrogen atom, C 1-C 12alkyl, C 1-C 12haloalkyl, C 1-C 6alkoxyC 1-C 6alkyl, C 1-C 6alkylthioC 1-C 6alkyl, C 3-C 12cycloalkyl, phenyl or phenyl substituted with (Z) p1, R **1c is C 1-C 12alkyl, C 1-C 6alkyl arbitrarily substituted with R **14, C 3-C 12cycloalkyl, C 3-C 12halocycloalkyl, C 3-C 8cyloalkyl arbitrarily substituted with R **14, E-3, E-5 to E-10, E-24 to E-29, E-31, E-32, E-35, E-46, C 3-C 12alkenyl, C 3-C 12haloalkenyl, C 3-C 6alkenyl arbitrarily substituted with R **14, C 3-C 12cydoalkenyl, C 3-C 12halocycloalkenyl, C 3-C 12alkynyl, C 3-C 12haloalkynyl, C 3-C 6alkynyl arbitrarily substituted with R **14, -N=C(R **17b)R **17a, phenyl, phenyl substituted with (Z) p1, D-1 to D-4, D-6 to D-13, D-15 to D-23, D-25 to D-37, D-39, D-40, D-42, D-43, D-45, D-47, D-50 to D-64 or D-65, R **1d is hydrogen atom, -C(O)R **15, -C(O)OR **15, -C(O)SR **15, -C(S)R **15, -C(S)OR **15, -C(S)SR **15 or -SO 2R **15,  R **1e is hydrogen atom, C 1-C 12alkyl, C 1-C 12haloalkyl, cyanoC 1-C 6alkyl, C 1-C 6alkoxyC 1-C 6alkyl, C 1-C 6alkylthio C 1-C 6alkyl, C 1-C 6alkylsulfonyl C 1-C 6alkyl, C 3-C 12alkenyl, C 3-C 12alkynyl or benzyl,  R **1f is -CHO, -C(O)R **15, -C(O)OR **15, -C(O)SR **15, -C(S)OR **15, -C(S)SR **15, -C(S)NH 2 or -C(S)N(R **16)R **15,  R **2 is cyano, C 1-C 12alkyl, -CH 2R **14a, E-5, E-7, E-9, E-24, E-27, E-30, C 3-C 12cycloalkenyl, C 3-C 12halocycloalkenyl, C 3-C 12alkynyl, C 3-C 12haloalkynyl, C 3-C 6alkynyl arbitrarily substituted with R **14a, -CHO, -C(O)R **15, -C(O)OR **15, -C(O)SR **15, -C(S)OR **15, -C(S)SR **15, -C(O)C(O)OR **15, -SR **15,-S(O) 2R **15, -S(O) 2N(R **16)R **15, -SN(R **20)R **19, phenyl or phenyl substituted with (Z) p1,  further when R **1 is -C(R **1b)=NOR **1a, M-5, M-20, M-48, or -C(R **1b)=NN(R **1e)R **1f, R **2 may be hydrogen atom, C 1-C 12haloalkyl, C 3-C 8cycloalkylC 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **14a, C 3-C 12alkenyl, C 3-C 12haloalkenyl or C 3-C 6alkenyl arbitrarily substituted with R **14a, when R **1 is -C(O)OR **1c, -C(O)SR **1c, -C(S)OR **1c or -C(S)SR **1c, R **2 may be hydrogen atom, halomethyl or -CH(R **14b)R **14a, when R **1 is -C(O)N(R **1e)R **1d or -C(S)N(R **1e)R **1d, R **2 may be hydrogen atom, C 1-C 12haloalkyl, C 3-C 8cycloalkylC 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **14a, C 3-C 12cycloalkyl, C 3-C 12halocycloalkyl, C 3-C 12alkenyl, C 3-C 12haloalkenyl or C 3-C 6alkenyl arbitrarily substituted with R **14a, when R **1 is phenyl, phenyl substituted with (Z) p1 or D-1 to D-65, R **2 may be C 1-C 12haloalkyl, C 3-C 8cycloalkylC 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **14a, C 3-C 12cycloalkyl, C 3-C 12halocycloalkyl, C 3-C 12alkenyl, C 3-C 12haloalkenyl, C 3-C 6alkenyl arbitrarily substituted with R **14a, -C(O)NH 2, -C(O)N(R **16)R **15, -OH, -OR **17, -N(R **18)R **17 or -N=C(R **17b)R **17a,  or R **2 together with R **1 may form =C(R **2b)R **2a, or further when substituent Y is present on an adjacent position, R **2 together with Y may form 5- or 6-membered ring together with the atoms to which the R **2 and Y are bonded by forming -CH 2-, -CH 2CH 2-, -CH 2O-, -CH 2S-, -CH 2N(R **6)-, -CH=CH- or -CH=N-, in this case, the hydrogen atom bonded to each carbon atom forming the ring may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkylidene, C 1-C 6haloalkylidene, oxo or thioxo, R **2a is hydrogen atom, -OR **1c, -SR **1c, C 1-C 6alkylsulfonyl, -NH 2, C 1-C 6alkylamino or di(C 1-C 6alkyl)amino,  R **2b is R **1b, C 1-C 6alkoxy, C 1-C 6haloalkoxy, phenoxy, phenoxy substituted with (Z) p1, C 1-C 6alkylthio, C 1-C 6haloalkylthio, -SCH 2R **14a, C 3-C 6alkenylthio, C 3-C 6haloalkenylthio, C 3-C 6alkynylthio, C 3-C 6haloalkynylthio, -SC(O)R **15, -SC(O)OR **15, phenylthio, phenylthio substituted  with (Z) p1 or di(C 1-C 6alkyl)amino,  R **3 is halogen atom, cyano, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **4, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with R **4, E-1 to E-50, C 3-C 6alkenyl, C 2-C 6alkenyl arbitrarily substituted with R **4, C 3-C 6alkynyl, C 2-C 6alkynyl arbitrarily substituted with R **4, -OR **5, -S(O) rR **5, -N(R **10)R **9, -N(R **10)R **9a, -CHO, -C(O)R **9, -C(O)OR **9, -C(O)SR **9, -C(O)NH 2, -C(O)N(R **10)R **9, -C(S)OR **9, -C(S)SR **9, -C(S)NH 2, -C(S)N(R **10)R **9, -CH=NOR **11, -C(R **9)=NOR **11, M-5, M-20, M-48, -Si(R **12a)(R **12b)R **12, -P(O)(OR **21) 2, phenyl, phenyl substituted with (Z) p1 or D-1 to D-65, D-1 to D-65 are aromatic heterocyclic rings of the following formulae, respectively (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) Z is halogen atom, cyano, nitro, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 4alkoxy C 1-C 4alkyl, C 1-C 4haloalkoxy C 1-C 4alkyl, C 1-C 4alkylthio C 1-C 4alkyl, C 1-C 4haloalkylthio C 1-C 4alkyl, C 1-C 4alkylsulfinyl C 1-C 4alkyl, C 1-C 4haloalkylsulfinyl C 1-C 4alkyl, C 1-C 4alkylsulfonyl C 1-C 4alkyl, C 1-C 4haloalkylsulfonyl C 1-C 4alkyl, C 3-C 6cycloalkyl, C 3-C 6halocycloalkyl, -OH, C 1-C 6alkoxy, C 1-C 6haloalkoxy, C 1-C 6alkylsulfonyloxy, C 1-C 6haloalkylsulfonyloxy, C 1-C 6alkylthio, C 1-C 6haloalkylthio, C 1-C 6alkylsulfinyl, C 1-C 6haloalkylsulfinyl, C 1-C 6alkylsulfonyl, C 1-C 6haloalkylsulfonyl, -NH 2, C 1-C 6alkylamino, di(C 1-C 6alkyl)amino, C 1-C 6alkoxycarbonyl, C 1-C 6haloalkoxycarbonyl, -C(O)NH 2, C 1-C 6alkylaminocarbonyl, C 1-C 6haloalkylaminocarbonyl, di(C 1-C 6alkyl)aminocarbonyl, -C(S)NH 2, -S(O) 2NH 2, C 1-C 6alkylaminosulfonyl, di(C 1-C 6alkyl)aminosulfonyl, phenyl or phenyl arbitrarily substituted with halogen atom, when p1, p2, p3 or p4 is an integer of 2 or more, each Z may be identical with or different from each other,  further, when two Zs are adjacent, the adjacent two Zs may form 5-membered or 6-membered ring together with carbon atoms to which the two Zs are bonded by forming -CH 2CH 2CH 2-, -CH 2CH 2O-, -CH 2OCH 2-, -OCH 2O-, -CH 2CH 2S-, -CH 2SCH 2-, -CH 2CH 2CH 2CH 2-, -CH 2CH 2CH 2O-, -CH 2CH 2OCH 2-, -CH 2OCH 2O-, -OCH 2CH 2O-, -CH 2CH 2CH 2S-, -OCH 2CH 2S- or -CH=CH-CH=CH-, in this case, hydrogen atoms bonded to each carbon atom forming the ring may be arbitrarily substituted with halogen atom, cyano, nitro, C 1-C 4alkyl, C 1-C 4haloalkyl, C 1-C 4alkoxy or C 1-C 4alkylthio, when R **1 is phenyl substituted with (Z) p1 or D-1 to D-65 and Z is present on an adjacent position of R **1 bonding position, Z together with R **2 may form 5- to 7-membered ring together with the carbon atom to which Z and R **2 are bonded by forming -CH 2CH 2-, -CH 2O-, -CH 2S-, -CH 2N(R **13)-, -CH 2CH 2CH 2-, -CH 2CH 2O-, -CH 2OCH 2-, -CH 2CH 2S-, -CH 2SCH 2-, -CH 2CH 2N(R **13)-, -CH 2N(R **13)CH 2-, -CH 2CH 2CH 2CH 2-, -CH 2CH 2CH 2O-, -CH 2CH 2CH 2S- or -CH 2CH 2CH 2N(R **13)-, in this case, the hydrogen atom bonded to each carbon atom forming the ring may be arbitrarily substituted with halogen atom, cyano, nitro, C 1-C 4alkyl, C 1-C 4haloalkyl, C 1-C 4alkoxy or C 1-C 6alkylthio, E-1 to E-50 are saturated heterocyclic rings of the following formulae, repectively (see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm) R **4 is halogen atom, cyano, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, E-5 to E-50, -OH, -OR **5, -SH, -S(O) rR **5, -N(R **7)R **6, -N(R **7)C(O)R **9a, -N(R **7)C(O)OR **9a, -N(R **7)C(O)SR **9a, -N(R **7)C(S)OR **9a, -N(R **7)C(S)SR **9a, -N(R **7)S(O) 2R **9a, -C(O)OR **9, -C(O)N(R **10)R **9, -Si(R **12a)(R **12b)R **12, phenyl, phenyl substituted with (Z) p1 or D-1 to D-65, R **5 is C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **24, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with R **24, E-3 to E-10, E-24 to E-32, E-35, E-46, C 2-C 6alkenyl, C 2-C 6alkenyl arbitrarily substituted with R **24, C 3-C 8cycloalkenyl, C 3-C 8halocycloalkenyl, C 3-C 6alkynyl, C 3-C 6alkynyl arbitrarily substituted with R **24, C 1-C 6alkylcarbonyl, C 1-C 6alkoxycarbonyl, phenyl, phenyl substituted with (Z) p1, D-1 to D-4, D-6 to D-13, D-15 to D-23, D-25 to D-37, D-39, D-40, D-42, D-43, D-45, D-47, D-50 to D-64 or D-65,  R **6 is C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **24, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl, C 3-C 6haloalkynyl, -CHO, -C(O)R **9, -C(O)OR **9, -C(O)SR **9, -C(O)NH 2, -C(O)N(R **10)R **9, -C(S)OR **9, -C(S)SR **9, -C(S)NH 2, -C(S)N(R **10)R **9, -C(O)C(O)R **9, -C(O)C(O)OR **9, -OH, -S(O) 2R **9, -S(O) 2N(R **10)R **9, -P(O)(OR **21) 2 or -P(S)(OR **21) 2,  R **7 is hydrogen atom, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **24, C 3-C 8cycloalkyl, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl, C 3-C 6haloalkynyl, -CHO, C 1-C 6alkylcarbonyl, C 1-C 6haloalkylcarbonyl or C 1-C 6alkoxycarbonyl, or R **7 together with R **6 may form 3- to 7-membered ring together with the nitrogen atom bonding them by forming C 2-C 6alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, oxo or thioxo,  R **8 is C 1-C 6alkyl, C 1-C 6haloalkyl, C 3-C 6alkenyl, phenyl or phenyl substituted with (Z) P1, R **9 is C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **24, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, E-1 to E-50, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl or C 3-C 6haloalkynyl,  R **9a is phenyl, phenyl substituted with (Z)p 1 or D-1 to D-65,  R **10 is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 3-C 6cycloalkyl C 1-C 4alkyl, C 1-C 6alkoxy C 1-C 4alkyl, C 1-C 6alkylthio C 1-C 4alkyl, cyano C 1-C 6alkyl, C 3-C 6alkenyl or C 3-C 6alkynyl, or R **10 together with R **9 may form 3- to 7-membered ring with the nitrogen atom bonding them by forming C 2-C 6alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6alkoxy, -CHO, C 1-C 6alkylcarbonyl or C 1-C 6alkoxycarbonyl,  R **11 is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, phenyl C 1-C 4alkyl, phenyl C 1-C 4alkyl substituted with (Z) P1, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl or C 3-C 6haloalkynyl,  R **12 is C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxy, phenyl or phenyl substituted with (Z) p1, R **12a and R **12b independently of each other are C 1-C 6alkyl, C 1-C 6haloalkyl or C 1-C 6alkoxy,  R **13 is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxycarbonyl C 1-C 4alkyl, C 1-C 6haloalkoxycarbonyl C 1-C 4alkyl, phenyl C 1-C 4alkyl, phenyl C 1-C 4alkyl substituted with (Z) p1, C 2-C 6alkenyl, C 2-C 6haloalkenyl, C 3-C 6alkynyl, C 3-C 6haloalkynyl, C 1-C 6alkoxy, C 1-C 6alkoxycarbonyl, C 1-C 6haloalkoxycarbonyl, phenyl or phenyl substituted with (Z) p1,  further, in case where Z is present in an adjacent position of R **13, the adjacent R **13 and Z may form 6-membered ring together with the atom bonding them by forming -CH 2CH 2CH 2CH 2-, -CH=CH-CH=CH-, -N=CH-CH=CH-, -CH=N-CH=CH-, -CH=CH-N=CH- or -CH=CH-CH=N-, in this case, hydrogen atoms bonded to each carbon atom forming the ring may be arbitrarily substituted with halogen atom, C 1-C 4alkyl or C 1-C 4haloalkyl,  R **14 is cyano, nitro, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, hydroxy C 3-C 6cycloalkyl, C 1-C 4alkoxy C 3-C 6cycloalkyl, E-10 to E-12, E-19, E-24 to E-29, E-31 to E-33, E-44, -OR **25, -N(R **26)R **25, -SH, -S(O) rR **27, C 5-C 8cycloalkenyl, C 5-C 8halocycloalkenyl, -CHO, -C(O)R **28, -C(O)OH, -C(O)OR **28, -C(O)SR **28, -C(O)NH 2, -C(O)N(R **29)R **28, -C(S)OR **28, -C(S)SR **28, -C(S)NH 2, -C(S)N(R **29)R **28, -CH=NOR **30, -C(R **28)=NOR **30, -C(=NR **29)OR **28, -C(=NR **29)SR **28, -C(=NR **29)N(R **29a)R **28a, -C(=NOR **30)N( R **29a)R **28a, -C(O)C(O)OR **28, -SO 2OH, -SO 2NH 2, -SO 2N(R **29)R **28, -Si(R **12a)(R **12b)R **12, -P(O)(OR **21) 2, -P(S)(OR **21) 2, -P(phenyl) 2, -P(O)(phenyl) 2, M-1 to M-48, phenyl, phenyl substituted with (Z) p1, naphthyl, D-1 to D-4, D-15 to D-17, D-21 to D-23, D-52 to D-58 or D-59, M-1 to M-48 are partially saturated heterocyclic rings of the following formulae, respectively (see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm)(see diagramm) R **14a is cyano, nitro, -OR **25, -N(R **26)R **25, -S(O) rR **27, -CHO, -C(O)R **28, -C(O)OR **28, -C(O)SR **28, -C(O)NH 2, -C(S)OR **28, -C(S)SR **28, -C(S)NH 2, -C(O)C(O)OR **28, -Si(R **12a)(R **12b)R **12, -P(O)(OR **21) 2, -P(S)(OR **21) 2 or phenyl, R **14b is C 1-C 6alkyl or C 3-C 6cycloalkyl,  R **15 is C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **31, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, E-1 to E-50, C 2-C 6alkenyl, C 2-C 6haloalkenyl, C 3-C 8cycloalkenyl, C 3-C 8halocycloalkenyl, C 2-C 6alkynyl, C 2-C 6haloalkynyl, phenyl, phenyl substituted with (Z) p1, naphthyl or D-1 to D-65,  R **16 is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 3-C 6cycloalkyl C 1-C 4alkyl, C 1-C 6alkoxy C 1-C 4alkyl, C 1-C 6alkylthio C 1-C 4alkyl, cyanoC 1-C 6alkyl, C 3-C 6alkenyl or C 3-C 6alkynyl, or R **16 together with R **15 may form 3- to 7-membered ring with the nitrogen atom bonding them by forming C 2-C 6alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6alkoxy, -CHO, C 1-C 6alkylcarbonyl or C 1-C 6alkoxycarbonyl,  R **17 is hydrogen atom, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **14, C 3-C 6cycloalkyl, C 3-C 8halocycloalkyl, E-6, E-8, E-10, E-25, E-26, E-28, E-29, E-31, E-32, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl, C 3-C 6haloalkynyl, -CHO, -C(O)R **28, -C(O)OR **28, -C(O)SR **28, -C(O)NH 2, -C(O)N(R **29)R **28, -C(S)OR **28, -C(S)SR **28, -C(S)NH 2, -C(S)N(R **29)R **28, -S(O) 2R **28, -S(O) 2NH 2, -S(O) 2N(R **29)R **28, -P(O)(OR **21) 2, -P(S)(OR **21) 2, phenyl, phenyl substituted with (Z) P1, D-1 to D-13, D-15 ro D-25, D-30 to D-37, D-42, D-43, D-45, D-50 to D-64 or D-65,  R **17a is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxy C 1-C 4alkyl, C 1-C 6alkylthio C 1-C 4alkyl, C 1-C 4alkylsulfonyl C 1-C 4alkyl, C 1-C 4alkoxycarbonyl C 1-C 4alkyl, phenyl C 1-C 4alkyl, phenyl C 1-C 4alkyl substituted with (Z) p1, C 3-C 6cycloalkyl, E-1 to E-50, phenyl C 2-C 4alkenyl, di(C 1-C 6alkyl)amino, phenyl, phenyl substituted with (Z) p1 or D-1 to D-65,  R **17b is hydrogen atom, C 1-C 6alkyl, C 1-C 6alkoxy, C 1-C 6alkylthio or di(C 1-C 6alkyl)amino, or R **17b together with R **17a may form 4- to 6-membered ring with the carbon atom bonding them by forming C 3-C 5alkylene chain or C 4-C 5alkenylene chain, in this case, the alkylene chain or the alkenylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, -CHO, C 1-C 6alkylcarbonyl or C 1-C 6alkoxycarbonyl,  R **18 is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxy C 1-C 4alkyl, C 1-C 4haloalkoxy C 1-C 4alkyl, C 1-C 4alkylthio C 1-C 4alkyl, C 1-C 4haloalkylthio C 1-C 4alkyl, C 1-C 4alkylsulfonyl C 1-C 4alkyl, C 1-C 6haloalkylsulfonyl C 1-C 4alkyl, cyanoC 1-C 6alkyl, C 1-C 4alkoxycarbonyl C 1-C 4alkyl, phenyl C 1-C 4alkyl, C 2-C 6alkenyl, C 2-C 6haloalkenyl, C 3-C 6alkynyl, C 3-C 6haloalkynyl, -CHO, -C(O)R **15, -C(O)OR **15, -C(O)SR **15, -C(S)OR **15, -C(S)SR **15, C 1-C 6alkylsulfonyl or C 1-C 6haloalkylsulfonyl, or R **18 together with R **17 may form 5- to 6-membered ring with the nitrogen atom bonding them by forming C 4-C 5alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with C 1-C 6alkyl, C 1-C 6alkoxy C 1-C 6alkyl, -CHO, C 1-C 6alkylcarbonyl or C 1-C 6alkoxycarbonyl, R **19 is C 1-C 12alkyl, C 1-C 12haloalkyl, C 1-C 12alkoxy C 1-C 12alkyl, cyanoC 1-C 12alkyl, C 1-C 12alkoxycarbonyl C 1-C 12alkyl, phenyl C 1-C 6alkyl, phenyl C 1-C 6alkyl substituted with (Z) p1, C 3-C 12alkenyl, C 3-C 12haloalkenyl, C 3-C 12alkynyl, C 3-C 12haloalkynyl, C 1-C 12alkylcarbonyl, C 1-C 12alkoxycarbonyl, -C(O)ON=C(CH 3)SCH 3, -C(O)ON=C(SCH 3)C(O)N(CH3) 2, phenyl or phenyl substituted with (Z) p1, R **20 is C 1-C 12alkyl, C 1-C 12haloalkyl, C 1-C 12alkoxy C 1-C 12alkyl, cyanoC 1-C 12alkyl, C 1-C 12alkoxycarbonyl C 1-C 12alkyl, phenyl C 1-C 6alkyl, phenyl C 1-C 6alkyl substituted with (Z) p1, C 3-C 12alkenyl, C 3-C 12haloalkenyl, C 3-C 12alkynyl, C 3-C 12haloalkynyl, phenyl or phenyl substituted with (Z) P1, or R **20 together with R **19 may form 5- to 8-membered ring with the nitrogen atom bonding them by forming C 4-C 7alkylene chain, in this case, the alkylene chain may contain one oxygen atom or sulfur atom, and may be arbitrarily substituted with C 1-C 4alkyl or C 1-C 4alkoxy,  R **21 is C 1-C 6alkyl or C 1-C 6haloalkyl,  R **22 is halogen atom, cyano, C 1-C 6alkyl, C 1-C 6haloalkyl, hydroxyC 1-C 6alkyl, C 1-C 4alkoxyC 1-C 4alkyl, C 1-C 4alkoxycarbonyl C 1-C 4alkyl, C 1-C 4alkoxy, C 1-C 6alkylthio, C 1-C 6alkylamino, di(C 1-C 4alkyl)amino, C 1-C 6alkoxycarbonyl, phenyl or phenyl substituted with (Z) p1, when q1 to q8 are integers of 2 or more, each R **22 may be identical with or different from each other, further, when two R **22s are present on the same carbon atom, the two R **22s together may form oxo, thioxo, imino, C 1-C 6alkylimino, C 1-C 6alkoxyimino or C 1-C 6alkylidene,  R **23 is hydrogen atom, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **31, C 3-C 6cycloalkyl, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl, -OH, benzyloxy, -CHO, -C(O)R **32, -C(O)OR **32, -C(O)SR **32, -C(O)NHR **33, -C(O)N(R **33)R **32, -C(S)NHR **33, -C(S)N(R **33)R **32, -S(O) 2R **32, -P(O)(OR **21) 2, -P(S)(OR **21) 2, phenyl, phenyl substituted with (Z) p1 or D-5,  R **24 is halogen atom, cyano, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, E-1 to E-50, C 1-C 6alkoxy, C 1-C 6haloalkoxy, C 1-C 6alkylthio, C 1-C 6haloalkylthio, C 1-C 6alkylsulfonyl, C 1-C 6haloalkylsulfonyl, C 1-C 6alkylamino, di(C 1-C 6alkyl)amino, -CHO, C 1-C 6alkylcarbonyl, C 1-C 6haloalkylcarbonyl, C 1-C 6alkoxycarbonyl, C 1-C 6haloalkoxycarbonyl, C 1-C 6alkylaminocarbonyl, di(C 1-C 6alkyl)aminocarbonyl, phenyl, phenyl substituted with (Z) p1, or D-1 to D-65,  R **25 is hydrogen atom, C 1-C 8alkyl, C 1-C 8alkyl arbitrarily substituted with R **31, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with R **31, E-3 to E-10,. E-24 to E-32, E-35, E-46, C 3-C 8alkenyl, C 3-C 8alkenyl arbitrarily substituted with R **31, C 3-C 8alkynyl, C 3-C 8alkynyl arbitrarily substituted with R **31, -CHO, -C(O)R **32, -C(O)OR **32, -C(O)SR **32, -C(O)NHR **33, -C(O)N(R **33)R **32, -C(S)R **32, -C(S)OR **32, -C(S)SR **32, -C(S)NHR **33, -C(S)N(R **33)R **32, -C(O)C(O)R **32, -C(O)C(O)OR **32, -SO 2R **32, -S(O) 2N(R **33)R **32, -Si(R **12a)(R **12b)R **12, -P(O)(OR **21) 2, -P(S)(OR **21) 2, phenyl, phenyl substituted with (Z) p1, D-1 to D-4, D-6 to D-13, D-15 to D-23, D-25 to D-37, D-39, D-40, D-42, D-43, D-45, D-47, D-50 to D-64 or D-65,  R **26 is hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 4alkoxy C 1-C 4alkyl, C 1-C 4alkylthio C 1-C 4alkyl, C 3-C 6cyclloalkyl, C 3-C 6alkenyl, C 3-C 6alkynyl, C 1-C 6alkoxy, phenyl or phenyl substituted with (Z) p1, or R **26 together with R **25 may form 3- to 7-membered ring with the nitrogen atom bonding them by forming C 2-C 6alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkoxy, -CHO, C 1-C 6alkylcarbonyl, C 1-C 6alkoxycarbonyl, phenyl, phenyl substituted with (Z) p1, oxo or thioxo,  R **27 is C 1-C 8alkyl, C 1-C 8alkyl arbitrarily substituted with R **31, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with  R **31, E-3, E-5 to E-10, E-24 to E-32, E-35, E-46, C 3-C 8alkenyl, C 3-C 8alkenyl arbitrarily substituted with R **31, C 3-C 8alkynyl, C 3-C 8alkynyl arbitrarily substituted with R **31, -CHO, -C(O)R **32, =C(O)OR **32, -C(O)SR **32, -C(O)NHR **33, -C(O)N(R **33)R **32, -C(S)R **32, -C(S)OR **32, -C(S)SR **32, -C(S)NHR **33, -C(S)N(R **33)R **32, -C(O)C(O)R **32, -C(O)C(O)OR **32, -SH, C 1-C 6alkylthio, C 1-C 8haloalkylthio, phenylthio, phenylthio substituted with (Z) p1, -P(O)(OR **21) 2, -P(S)(OR **21) 2, phenyl or phenyl substituted with (Z) P1, D-18, D-21, D-25, D-30 to D-35, D-50, D-52, D-55 or D-56,  R **28 and R **28a independently of each other are C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **31, C 3-C 8cycloalkyl, C 3-C 8cycloalkyl arbitrarily substituted with R **31, C 2-C 8alkenyl C 3-C 8cycloalkyl, C 2-C 6haloalkenyl C 3-C 8cycloalkyl, E-1 to E-50, C 2-C 8alkenyl, C 2-C 8alkenyl arbitrarily substituted with R **31, C 2-C 8alkynyl, C 2-C 8alkynyl arbitrarily substituted with R **31, phenyl, phenyl substituted with (Z) p1 or D-1 to D-65,  R **29 and R **29a independently of each other are hydrogen atom, C 1-C 6alkyl, C 1-C 6alkyl arbitrarily substituted with R **31, C 3-C 6alkenyl, C 3-C 6haloalkenyl, C 3-C 6alkynyl, C 3-C 6haloalkynyl, phenyl or phenyl substituted with (Z) p1, or R **29 together with R **28 may form 3- to 6-membered ring with the nitrogen atom bonding them by forming C 2-C 5alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6alkoxy, -CHO, C 1-C 6alkylcarbonyl, C 1-C 6alkoxycarbonyl, phenyl or phenyl substituted with (Z) p1,  R **30 is C 1-C 8alkyl, C 1-C 8alkyl arbitrarily substituted with R **31, C 3-C 8cycloalkyl, C 3-C 8alkenyl, C 3-C 8alkenyl arbitrarily substituted with R **31, C 3-C 8alkynyl or C 3-C 8alkynyl arbitrarily substituted with R **31, R **31 is halogen atom, cyano, nitro, C 3-C 8cycloalkyl, C 3-C 8halocycloalkyl, E-5 to E-8, E-11 to E-15, E-19, E-20, E-24 to E-29, E-33 to E-39, E-44 to E-46, -OH, -OR **32, -OC(O)R **32, -OC(O)OR **32;  -OC(O)NHR **33, -OC(O)N(R **33)R **32, -OC(S)NHR **33, -OC(S)N(R **33)R **32, -SH, -S(O),R **32, -SC(O)R **32, -SC(O)OR **32, -SC(O)NHR **33, -SC(O)N(R **33)R **32, -SC(S)NHR **33, -SC(S)N(R **33)R **32, -NHR **33, -N(R **33)R **32, -N(R **33)CHO, -N(R **33)C(O)R **32, -N(R **33)C(O)OR **32, -N(R **33)C(O)NHR **33a, -N(R **33)C(O)N(R **33a)R **32, -N(R **33)C(S)NHR **33a, -N(R **33)C(S)N(R **33a)R **32, -CHO, -C(O)R **32, -C(O)OH, -C(O)OR **32, -C(O)SR **32, -C(O)NHR **33, -C(O)N(R **33)R **32, -C(O)C(O)OR **32, -Si(R **12a)(R **12b)R **12, -P(O)(OR **21) 2, -P(S)(OR **21) 2, -P(phenyl) 2, -P(O)(phenyl) 2, phenyl, phenyl substituted with (Z) p1, or D-1 to D-65,  R **32 is C 1-C 6alkyl, C 1-C 6haloalkyl, C 1-C 6alkyl arbitrarily substituted with R **34, C 3-C 6cycloalkyl, C 3-C 6halocycloalkyl, C 2-C 6alkenyl C 3-C 8cycloalkyl, C 2-C 6haloalkenyl C 3-C 8cycloalkyl, E-5 to E-8, E-24 to E-29, C 2-C 8alkenyl, C 2-C 8haloalkenyl, C 3-C 8cycloalkenyl, C 3-C 8halocycloalkenyl, C 2-C 8alkynyl, C 2-C 6haloalkynyl, phenyl, phenyl substituted with (Z) p1 or D-1 to D-65,  R **33 and R **33a independently of each other are hydrogen atom, C 1-C 6alkyl, C 1-C 6haloalkyl, C 3-C 8cycloalkyl, C 3-C 6alkenyl, C 3-C 6alkynyl, C 1-C 6alkylcarbonyl, C 1-C 6haloalkylcarbonyl, C 1-C 6alkoxycarbonyl, C 1-C 6haloalkoxycarbonyl, phenoxycarbonyl, phenoxycarbonyl substituted with (Z) p1, phenylcarbonyl, phenylcarbonyl substituted with (Z) p1, C 1-C 6alkylsulfonyl, C 1-C 6haloalkylsulfonyl, phenyl, phenyl substituted with (Z) P1, D1 to D-4, D-6 to D-13, D-15 to D-23, D-25 to D-37, D-39, D-40, D-42, D-43, D-45, D-47, D-50 to D-64 or D-65, or R **33 together with R **32 may form 3- to 6-membered ring with the nitrogen atom bonding them by forming C 2-C 5alkylene chain, in this case, the alkylene chain may contain one oxygen atom, sulfur atom or nitrogen atom, and may be arbitrarily substituted with halogen atom, C 1-C 6alkyl, C 1-C 6alkoxy, -CHO, C 1-C 6alkylcarbonyl, C 1-C 6alkoxycarbonyl, phenyl or phenyl substituted with (Z) P1,  R **34 is cyano, C 3-C 6cycloalkyl, C 3-C 6halocycloalkyl, E-5 to E-8, E-24 to E-29, C 1-C 4alkoxy, C 1-C 4haloalkoxy, phenoxy, phenoxy substituted with (Z) p1, C 1-C 4alkylthio, C 1-C 4haloalkylthio, C 1-C 4alkylsulfonyl, C 1-C 4haloalkylsulfonyl, phenylthio, phenylthio substituted with (Z) P1, -N(R **36)R **35, C 1-C 6alkylcarbonyl, C 1-C 6haloalkylcarbonyl, C 1-C 6alkoxycarbonyl, di(C 1-C 6alkyl)aminocarbonyl, tri(C 1-C 4alkyl)silyl, phenyl, phenyl substituted with (Z) P1, naphthyl or D-1 to D-65, R **35 is hydrogen atom, C 1-C 6alkyl, C 1-C 6alkylcarbonyl, C 1-C 6haloalkylcarbonyl, C 1-C 6alkoxycarbonyl, phenylcarbonyl or phenylcarbonyl substituted with (Z) p1,  R **36 is hydrogen atom or C 1-C 6alkyl,  m is an integer of 0 to 5,  n is an integer of 0 to 4,  p1 is an integer of 1 to 5,  p2 is an integer of 0 to 4,  p3 is an integer of 0 to 3,  p4 is an integer of 0 to 2,  p5 is an integer of 0 or 1,  q1 is an integer of 0 to 3,  q2 is an integer of 0 to 5,  q3 is an integer of 0 to 7,  q4 is an integer of 0 to 9,  q5 is an integer of 0 to 6,  q6 is an integer of 0 to 4,  q7 is an integer of 0 to 2,  q8 is an integer of 0 to 8,  r is an integer of 0 to 2, and  t is an integer of 0 or 1. 2. The isox(...)
法律状态
(EP1932836) LEGAL DETAILS FOR EP1932836  Actual or expected expiration date=2026-09-01    Legal state=ALIVE    Status=GRANTED     Event publication date=2006-09-01  Event code=EP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=EP EP06797653  Application date=2006-09-01  Standardized application number=2006EP-0797653     Event publication date=2008-06-18  Event code=EP/A1  Event type=Examination events  Application published with search report  Publication country=EP  Publication number=EP1932836  Publication stage Code=A1  Publication date=2008-06-18  Standardized publication number=EP1932836     Event publication date=2008-06-18  Event code=EP/17P  Event indicator=Pos  Event type=Examination events  Request for examination filed Pruefungsantrag gestellt  Effective date of the event=2008-03-18     Event publication date=2008-06-18  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 HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR    Event publication date=2008-06-18  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 BA HR MK RS    Event publication date=2009-11-04  Event code=EP/A4  Event indicator=Pos  Event type=Examination events  Supplementary search report Ergaenzender recherchenbericht  Publication country=EP  Publication number=EP1932836  Publication stage Code=A4  Publication date=2009-11-04  Standardized publication number=EP1932836     Event publication date=2009-11-04  Event code=EP/A4  Event indicator=Pos  Event type=Administrative notifications  Supplementary search report Despatch of supplementary search report  Effective date of the event=2009-10-07     Event publication date=2010-03-17  Event code=EP/17Q  Event indicator=Pos  Event type=Examination events  First examination report Erster pruefungsbescheid  Effective date of the event=2010-02-15     Event publication date=2013-08-14  Event code=EP/INTG  Event indicator=Pos  Event type=Examination events  Announcement of intention to grant  Effective date of the event=2013-07-16     Event publication date=2013-11-06  Event code=EP/B1  Event indicator=Pos  Event type=Event indicating In Force  Patent specification  Publication country=EP  Publication number=EP1932836  Publication stage Code=B1  Publication date=2013-11-06  Standardized publication number=EP1932836     Event publication date=2013-11-06  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 HU IE IS IT LI LT LU LV MC NL PL PT RO SE SI SK TR    Event publication date=2013-11-06  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 BA HR MK RS    Event publication date=2014-10-15  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=2014-08-07  MEMBER STATE LEGAL DETAILS FOR AT  Actual or expected expiration date=2013-11-06    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=AT Corresponding appl: AT639397    Event publication date=2013-12-15  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=2013-12-15     Event publication date=2014-03-15  Event code=EP/REG  Event code=AT/MK05  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Revocation of the translation of the ep patent Loeschung gemaess par. 5 (zurueckziehung der uebersetzung des ep patents) Corresponding cc:  Designated or member state=AT   Effective date of the event=2013-11-06     Event publication date=2014-05-30  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=AT  MEMBER STATE LEGAL DETAILS FOR BE  Actual or expected expiration date=2014-05-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=BE     Event publication date=2014-05-30  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=BE  MEMBER STATE LEGAL DETAILS FOR BG  Actual or expected expiration date=2016-05-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=BG     Event publication date=2016-05-31  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=BG  MEMBER STATE LEGAL DETAILS FOR CH  Actual or expected expiration date=2015-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CH     Event publication date=2013-11-15  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=2015-04-30  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     Event publication date=2015-07-31  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=CH  MEMBER STATE LEGAL DETAILS FOR CY  Actual or expected expiration date=2016-06-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CY     Event publication date=2016-06-30  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=2014-08-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CZ     Event publication date=2014-08-29  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=CZ  MEMBER STATE LEGAL DETAILS FOR DE  Actual or expected expiration date=2026-09-01    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=DE Corresponding appl: DE602006039167    Event publication date=2014-01-02  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   Effective date of the event=2014-01-02     Event publication date=2014-08-07  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=2014-11-13  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   Effective date of the event=2014-08-07     Event publication date=2017-09-22  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=2017-09-22     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=DE  MEMBER STATE LEGAL DETAILS FOR DK  Actual or expected expiration date=2014-09-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=DK     Event publication date=2014-09-30  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=DK  MEMBER STATE LEGAL DETAILS FOR EE  Actual or expected expiration date=2014-07-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=EE     Event publication date=2014-07-31  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=EE  MEMBER STATE LEGAL DETAILS FOR ES2443690  Actual or expected expiration date=2026-09-01    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=ES Corresponding appl: ES06797653  Application date in the designated or member state=2006-09-01   Application number in the designated or member state=2006ES-0797653T Corresponding cc:  Designated or member state=ES Corresponding pat: ES2443690  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2014-02-20   Publication number in the designated or member state=ES2443690    Event publication date=2014-02-20  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=2014-02-20     Event publication date=2017-10-02  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=2017-10-02     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=ES  MEMBER STATE LEGAL DETAILS FOR FI  Actual or expected expiration date=2014-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=FI     Event publication date=2014-04-30  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 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=2026-09-01    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=FR     Event publication date=2015-09-17  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=2015-09-17     Year of payment of annual fees=10  Corresponding cc:  Designated or member state=FR     Event publication date=2016-09-15  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=2016-09-15     Year of payment of annual fees=11  Corresponding cc:  Designated or member state=FR     Event publication date=2017-09-11  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=2017-09-11     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=FR     Event publication date=2017-09-11  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=2017-09-11     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=FR  MEMBER STATE LEGAL DETAILS FOR GB  Actual or expected expiration date=2026-09-01    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=GB     Event publication date=2013-11-06  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=2017-09-08  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=2017-09-08     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=GB  MEMBER STATE LEGAL DETAILS FOR GR  Actual or expected expiration date=2016-06-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=GR     Event publication date=2016-06-30  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=GR  MEMBER STATE LEGAL DETAILS FOR HU  Actual or expected expiration date=2016-07-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=HU     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  INVALID AB INITIO  Corresponding cc:  Designated or member state=HU  MEMBER STATE LEGAL DETAILS FOR IE  Actual or expected expiration date=2015-06-17    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IE     Event publication date=2013-12-18  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=2015-06-17  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=2015-08-31  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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=IE  MEMBER STATE LEGAL DETAILS FOR IS  Actual or expected expiration date=2014-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IS     Event publication date=2014-04-30  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 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=2026-09-01    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=IT     Event publication date=2017-09-06  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=2017-09-06     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=IT  MEMBER STATE LEGAL DETAILS FOR LI  Actual or expected expiration date=2015-07-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LI     Event publication date=2015-07-31  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=LI  MEMBER STATE LEGAL DETAILS FOR LT  Actual or expected expiration date=2014-04-25    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LT     Event publication date=2014-04-25  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     Event publication date=2014-04-30  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 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  MEMBER STATE LEGAL DETAILS FOR LU  Actual or expected expiration date=2015-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LU     Event publication date=2015-04-30  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 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=2014-05-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LV     Event publication date=2014-05-30  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=LV  MEMBER STATE LEGAL DETAILS FOR MC  Actual or expected expiration date=2015-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=MC     Event publication date=2015-04-30  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 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 NL  Actual or expected expiration date=2013-11-06    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=NL     Event publication date=2014-03-12  Event code=EP/REG  Event code=NL/VDEP  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Invalid in the netherlands as no translation has been filed Verval wegens niet indienen vertaling Corresponding cc:  Designated or member state=NL   Effective date of the event=2013-11-06     Event publication date=2014-04-30  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 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=NL  MEMBER STATE LEGAL DETAILS FOR PL  Actual or expected expiration date=2014-08-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=PL     Event publication date=2014-08-29  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=PL  MEMBER STATE LEGAL DETAILS FOR PT  Actual or expected expiration date=2014-06-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=PT     Event publication date=2014-06-30  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=PT  MEMBER STATE LEGAL DETAILS FOR RO  Actual or expected expiration date=2014-08-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=RO     Event publication date=2014-08-29  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=RO  MEMBER STATE LEGAL DETAILS FOR SE  Actual or expected expiration date=2014-04-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SE     Event publication date=2014-04-30  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 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=SE  MEMBER STATE LEGAL DETAILS FOR SI  Actual or expected expiration date=2015-02-27    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SI     Event publication date=2015-02-27  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=2014-08-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=SK     Event publication date=2014-08-29  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=SK  MEMBER STATE LEGAL DETAILS FOR TR  Actual or expected expiration date=2016-07-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=TR     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=TR
专利类型码
A1A4B1
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