Hydrazide compound and pesticidal use of the same 机翻标题: 暂无翻译,请尝试点击翻译按钮。

公开号/公开日
EP1937664 A1 2008-07-02 [EP1937664]EP1937664 B1 2011-06-15 [EP1937664] / 2008-07-022011-06-15
申请号/申请日
2006EP-0811793 / 2006-10-10
发明人
IKEGAMI HIROSHI;JACHMANN MARKUS;NOKURA YOSHIHIKO;IWATA CHIEMI;
申请人
SUMITOMO CHEMICAL;
主分类号
IPC分类号
A01N-043/36A01N-043/40A01N-043/56C07D-207/34C07D-231/14C07D-401/04C07D-401/14C07D-403/04C07D-413/14C07D-417/14
摘要
(EP1937664) A hydrazide compound represented by the formula (1): has excellent pesticidal activity.
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-0299843 2005-10-14 2006JP-0144829 2006-05-25 2006WO-JP320522 2006-10-10
主权利要求
(EP1937664) 1. A hydrazide compound represented by the formula (1) : (see diagramm) wherein,  R **1 represents a hydrogen atom; a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C2-C6 cyanoalkyl group; a C2-C6 alkoxyalkyl group optionally substituted with at least one halogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; a C3-C6 alkynyl group optionally substituted with at least one halogen atom; or a C7-C9 phenyl alkyl group whose benzene ring moiety may be substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom,  R **2 and R **3 independently represent a hydrogen atom; a C1-C6  alkyl group optionally substituted with at least one halogen atom; a C1-C6 acyl group; a C2-C6 alkoxycarbonyl group; a C3-C7 N,N-dialkylcarbamoyl group; or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group and (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom,  R **4 represents a halogen atom; a cyano group; a nitro group; a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a phenyl group optionally substituted with at least one halogen atom; a CI-CG alkylthio group optionally substituted with at least one halogen atom; a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom; or a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, or two R **4 groups which are bound to the adjacent carbon atoms are bound at their terminal ends to each other to form a group T1 or T2 T1 : -CR **41=CR **42-CR **43=CR **44-  T2 : (CR **45R **46) h-  (wherein R **41, R **42, R **43 and R **44 independently represent a hydrogen atom; a halogen atom; a cyano group; a nitro group; a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a C1-C6 alkylthio group optionally substituted with at least one halogen atom; a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom; or a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom,  R **45 and R **46 independently represent a hydrogen atom; or a C1-C5 alkyl group optionally substituted with at least one halogen atom, and  h represents an integer of 3 or 4),  n represents an integer of 0 to 4 (provided that, when n is an integer of 2 or more, R **4s may be the same or different),  Q represents a group selected from Q1 to Q6 :            Q1:     -C(=A **31)-R **5            Q2:     -C(=A **32)-OR **8            Q3:     -C(=A **33)-SR **7            Q4:     -C(=A **34)-NR **8R **9            Q5:     -S(O) 2-R **10            Q6:     -S(O) 2-NR **11R **12    (wherein A **31, A **32, A **33 and A **34 represent an oxygen atom or a sulfur atom,  R **5 represents a hydrogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; a C1-C6 alkyl group optionally substituted with one or more independent, substituents selected from the group consisting of (1) a halogen atom, (2) a C1-C6 alkoxy group, (3) a C1-C6 alkylthio group, (4) a C1-C6 alkylsulfinyl group, (5) a C1-C6 alkylsulfonyl group, (6) a C2-C6 dialkylamino group and (7) a C3-C6 cycloalkyl group; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino group optionally substituted with at least one halogen atom and (10) a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom; a naphthyl group optionally substituted with 1 to 9 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C5 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a 3- to 8-membered non-aromatic heterocyclic group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a C7-C9 phenylalkyl group whose benzene ring moiety may be substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; or a C7-C9 phenoxyalkyl group whose benzene ring moiety may be substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom,  R **6 and R **7 represent a C1-C5 alkyl group optionally substituted with at least one halogen atom; a C3-C6 alkoxyalkyl group optionally substituted with at least one halogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; a C3-C6 alkynyl group optionally substituted with at least one halogen atom; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino group optionally substituted with at least one halogen atom and (10) a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom;  or a C7-C9 phenylalkyl group whose benzene ring moiety may be substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C5 alkoxy group optionally substituted with at least one halogen atom,  R **8 and R **9 independently, represent a hydrogen atom; a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C2-C6 alkoxyalkyl group optionally substituted with at least one halogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; a C3-C6 alkynyl group optionally substituted with at least one halogen atom; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino group optionally substituted with at least one halogen atom and (10) a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with 1 to 5 independent substituent selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; or a C7-C9 phenylalkyl group whose benzene ring moiety may be substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; or R **8 and R **9 are taken together with the nitrogen atom to which they are bound to form a 3- to 8-membered non-aromatic heterocyclic group, the 3 to 8-membered non-aromatic heterocyclic group may contain, in the ring, one or more independent groups selected from the group consisting of (1) an oxygen atom, (2) a sulfur group and (3) a -NR **a- group (wherein R **a represents a C1-C6 alkyl group optionally substituted with at least one halogen atom, a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom, or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C5 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom), or carbon atom(s) in the ring may be substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (3) a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom,  R **10 represents a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of .(1) a halogen atom and (2) a C1-C6 alkyl group optionally substituted with at least one halogen atom; or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, and  R **11 and R **12 independently represent a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group optionally substituted with at least one halogen atom; or a phenyl group optionally substituted with I to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; or R **11 and R **12 are taken together with the nitrogen atom to which they are bound to form a 3- to 8-members non-aromatic heterocyclic group, the 3- to 8-membered non-aromatic heterocyclic group may contain, in the ring, one or more independent groups selected from the group consisting of (1) an oxygen atom, (2) a sulfur atom and (3) a -NR **b-group (wherein R **b represents a C1-C6 alkyl group optionally substituted with at least one halogen atom, a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom, or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-Cc alkoxy group optionally substituted with at least one halogen atom), and carbon atom(s) in the ring may be substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (3) a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom),  J represents a group represented by J1 or J2: (see diagramm) (wherein X **a, Y **a, Z **a, X **b, Y **b and Z **b independently represent CH or a nitrogen atom,  R **13a and R **13b represent a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C2-C6 cyanoalkyl group; a C2-C6 alkoxyalkyl group optionally substituted with at least one halogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; a C2-C6 alkynyl group optionally substituted with at least one halogen atom; a C3-C6 cycloalkyl group optionally substitute with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom and (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a C7-C9 phenylalkyl group whose benzene ring moiety may be substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom;  or a C7-C9 pyridinylalkyl group whose pyridine ring moiety may be substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group, optionally substituted with at least one halogen atom,  R **14a and R **14b represent a halogen atom; a cyano group; a nitro group; an isocyanato group; a C1-Cc alkyl group optionally substituted with at least one halogen a tom; a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a C2-C6 cyanoalkyloxy group; a C3-C6 alkoxyalkyloxy group optionally substituted with at least one halogen atom; a C3-C6 alkenyloxy group optionally substituted with at least one halogen atom; a C3-C6 alkynyloxy group optionally substituted with at least one halogen atom; a C1-C6 alkylthio group optionally substituted with at least one halogen atom; a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom; a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; or a phenoxy group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom,  p represents an integer of 0 to 3, and  q represents an integer of 0 to 3 (provided that, when p is an integer of 2 or 3, two or more R **14a's may be the same or different and, when q is an integer of 2 or 3, two or more R **14b's may be the same or different), and  A **1 and A **2 independently represent an oxygen atom or a sulfur atom. 2. The compound according to claim 1, wherein n is an integer of 0 to 3. 3. The compound according to claim 2, wherein R **4 is a halogen atom; a cyano group; a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C1-C6 alkoxy group optionally substituted with at least one halogen atom, or a phenyl group optionally substituted with at least one halogen atom, or two R **4 groups which are bound to the adjacent carbon atoms are bound at their terminal ends to form a group T1:            -CR **41=CR **42-CR **43=CR **44-    (wherein R **41, R **42, R **43 and R **44 represent a hydrogen atom). 4. The compound according to claim 3, wherein R **4 is a fluorine atoms; a chlorine atom; a bromine atom, an iodine atom; a cyano group; a methyl group; an ethyl group; a trifluoromethyl group; a methoxy group; a phenyl group, or two R **4 groups which are bound to the adjacent carbon atoms are bound at their terminal ends to form a group T1: -CR **41=CR **42-CR **43=CR **44-(wherein R **41 , R **42 , R **43 and R **44 represent a hydrogen atom). 5. The.compound according to claim 1, wherein  J is J1,  Y **a is CH,  R **13a is a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C5 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom and (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom; or a 5 to 6-membered heteroaryl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro croup, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom,  R **14a is a halogen atom; a cyano group; a C1-C6 alkyl group optionally substitute with at least one halogen atom; a C1-C6 alkylthio group optionally substituted with at least one halogen atom; a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom; a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom; or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; and  p is an integer of 0 to 2. 6. The compound according to claim 1, wherein  J is J2, Y **b is CH,  R **13b is a C1-C6 alkyl group optionally substituted with at least one halogen atom,  R **14b is a C1-C6 alkyl group optionally substituted with at least one halogen atom, or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, and  q is 1. 7. The compound according to claim 1, wherein A **1 and A **2 are an oxygen atom, and R **1 is a hydrogen atom or a methyl group. 8. The compound according to claim 1, wherein  Q is Q1,  A **31 is an oxygen atom, and  R **5 is a hydrogen atom; a C1-C6 alkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a C1-C6 alkoxy group, (3) a C1-C6 alkylthio group, (4) a C1-C6 alkylsulfinyl group, (5) a C1-C6 alkylsulfonyl group, (6) a C2-C6 dialkylamino group and (7) a C3-C6 cycloalkyl group; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino group optionally substituted with at least one halogen atom and (10) a C2-C6 alkoxycarbonyl group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom and (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom; or a 3- to 8-membered non-aromatic heterocyclic group optionally substituted with one or more independent groups selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group. 9. The compound according to claim 8, wherein R **5 is a hydrogen atom; a methyl group; an ethyl group; a tert-butyl group; a cyclopropyl group; a phenyl group; a 3-methylphenyl group; a 4-methoxyphenyl group; at 2-pyridinyl group, or a morpholino group. 10. The compound according to claim 1, wherein  Q is Q2,  A **32 is an oxygen atom, and  R **6 is a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C2-C6 alkenyl group optionally substituted with at least one halogen atom; or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino croup optionally substituted with at least one halogen atom and (10) a C2-C6 alkoxy carbonyl group optionally substituted with at least one halogen atom. 11. The compound according to claim 10, wherein R **6 is a methyl group; an ethyl group; a propyl group; an isopropyl group; a butyl group; a sec-butyl group; a 2-propenyl group, or a phenyl group. 12. The compound according to claim 1, wherein  Q is Q4,  A **34 is an oxygen atom, and  R **8 and R **9 independently represent a hydrogen atom; a C1-C6 alkyl group optionally substituted with at least one halogen atom; or a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino group optionally substituted with at least one halogen atom and (10) a C2-C6 alkoxy carbonyl group optionally substituted with at least one halogen atom. 13. The compound according to claim 12, wherein R **8 and R **9 independently represent a hydrogen atom; a methyl group; an ethyl group, or a phenyl group. 14. The compound according to claim 1, wherein R **2 is a hydrogen atom or a methyl group, and R **3 is a hydrogen atom, a methyl group, an isopropyl group, or a methoxycarbonyl group. 15. The compound according to claim 1, wherein  R **1 is a hydrogen atom, or a C1-C6 alkyl group optionally substituted with at least one halogen atom,  R **2 is a hydrogen atom, or a C1-C6 alkyl group optionally substituted with at least one halogen atom,  R **3 is a hydrogen atom, a C1-C-6 alkyl group optionally substituted with at least one halogen atom, or a C2-C6 alkoxycarbonyl group,  R **4 is a halogen atom; a cyano group; a C1-C6 alkyl group optionally substituted with at least one halogen atom; a C1-C6 alkoxy group optionally substituted with at least one halogen atom; a phenyl group optionally substituted with at least one halogen atom, or  two R **4 groups which are bound to the adjacent carbon atoms are bound at their terminal ends to form a group T1:            -CR **41=CR **42-CR **43=CR **44-    (wherein R **41, R **42, R **43 and R **44 represent a hydrogen atom),  n is an integer of 0 to 3,  Q is a group selected from Q1 to Q6:            Q1:     -C(=A **31)-R **5            Q2:     -C(=A **32)-OR **6            Q3:     -C(=A **33)-SR **7            Q4:     -C(=A **34)-NR **8R **8            Q5:     -S(O) 2R **10            Q6:     -S(O) 2-NR **11R **12    (wherein A **31, A **32 and A **33 are an oxygen atom, A **34 is an oxygen atom or a sulfur atom,  R **5 is a hydrogen atom; a C1-C6 alkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom, (2) a C1-C6 alkoxy group, (3) a C1-C6 alkylthio group, (4) a C1-C6 alkylsulfinyl group, (5) a C1-C6 alkylsulfonyl group, (6) a C2-C6 dialkylamino group and (7) a C3-C6 cycloalkyl group; a C3-C6 cycloalkyl group optionally substituted with one or more independent substituents selected from the group consisting of (1) a halogen atom and (2) a C1-C6 alkyl group; a phenyl group optionally substituted with 1 to 5 independent substituents selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C1-C6 alkyl group optionally substituted with at least one halogen atom, (5) a C1-C6 alkoxy group optionally substituted with at least one halogen atom, (6) a C1-C6 alkylthio group optionally substituted with at least one halogen atom, (7) a C1-C6 alkylsulfinyl group optionally substituted with at least one halogen atom, (8) a C1-C6 alkylsulfonyl group optionally substituted with at least one halogen atom, (9) a C2-C6 dialkylamino group optionally substituted with at least one halogen atom and (10) a C2-C6.alkoxycarbonyl group optionally substituted with at least one halogen atom; a 5- to 6-membered heteroaryl group optionally substituted with one or more independent substituent selected from the group consisting of (1) a halogen atom, (2) a cyano group, (3) a nitro group, (4) a C(...)
法律状态
(EP1937664) LEGAL DETAILS FOR EP1937664  Actual or expected expiration date=2026-10-10    Legal state=ALIVE    Status=GRANTED     Event publication date=2006-10-10  Event code=EP/APP  Event indicator=Pos  Event type=Examination events  Application details  Application country=EP EP06811793  Application date=2006-10-10  Standardized application number=2006EP-0811793     Event publication date=2008-07-02  Event code=EP/A1  Event type=Examination events  Application published with search report  Publication country=EP  Publication number=EP1937664  Publication stage Code=A1  Publication date=2008-07-02  Standardized publication number=EP1937664     Event publication date=2008-07-02  Event code=EP/17P  Event indicator=Pos  Event type=Examination events  Request for examination filed Pruefungsantrag gestellt  Effective date of the event=2008-03-27     Event publication date=2008-07-02  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=2009-04-29  Event code=EP/17Q  Event indicator=Pos  Event type=Examination events  First examination report Erster pruefungsbescheid  Effective date of the event=2009-03-25     Event publication date=2010-11-17  Event code=EP/DAX  Event indicator=Neg  Event type=Designated states  Request for extension of the european patent (to any country) deleted    Event publication date=2011-06-15  Event code=EP/B1  Event indicator=Pos  Event type=Event indicating In Force  Patent specification  Publication country=EP  Publication number=EP1937664  Publication stage Code=B1  Publication date=2011-06-15  Standardized publication number=EP1937664     Event publication date=2011-06-15  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=2012-05-23  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=2012-03-16  MEMBER STATE LEGAL DETAILS FOR AT512958  Actual or expected expiration date=2015-10-10    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=AT Corresponding appl: AT06811793  Application date in the designated or member state=2006-10-10   Application number in the designated or member state=2006AT-0811793T Corresponding cc:  Designated or member state=AT Corresponding pat: AT512958  Publication stage code in the designated or member state=T  Publication date in the designated or member state=2011-07-15   Publication number in the designated or member state=ATE512958    Event publication date=2014-09-25  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=2014-09-25     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=AT     Event publication date=2016-06-15  Event code=EP/REG  Event code=AT/MM01  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Lapse because of not paying annual fees Loeschung wegen nichtzahlung der jaehrlichen gebuehr Corresponding cc:  Designated or member state=AT   Effective date of the event=2015-10-10     Event publication date=2016-08-31  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=AT  MEMBER STATE LEGAL DETAILS FOR BE  Actual or expected expiration date=2017-07-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=BE     Event publication date=2014-10-13  Event code=EP/PGFP  Event indicator=Pos  Event type=Event indicating In Force  Event type=Payment or non-payment notifications  Postgrant: annual fees paid to national office   Annual fees payment date=2014-10-13     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=BE     Event publication date=2017-07-31  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=BE  MEMBER STATE LEGAL DETAILS FOR BG  Actual or expected expiration date=2016-10-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=BG     Event publication date=2014-09-17  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=2014-09-17     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=BG     Event publication date=2016-10-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=BG  MEMBER STATE LEGAL DETAILS FOR CH  Actual or expected expiration date=2016-05-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CH     Event publication date=2011-06-15  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=2011-07-15  Event code=EP/REG  Event code=CH/NV  Event type=Change of name or address  Reference to a national code New agent Neuer vertreter/nouveaux mandataires/nuovi mandatari Corresponding cc:  Designated or member state=CH     Event publication date=2014-07-15  Event code=EP/REG  Event code=CH/PCAR  Event type=Change of name or address  Reference to a national code Change of the address of the representative Adressaenderung vertreter Corresponding cc:  Designated or member state=CH  NEW ADDRESS: HOLBEINSTRASSE 36-38, 4051 BASEL (CH)     Event publication date=2014-10-14  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=2014-10-14     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=CH     Event publication date=2016-05-31  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=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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=CH  MEMBER STATE LEGAL DETAILS FOR CY  Actual or expected expiration date=2011-11-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CY     Event publication date=2011-11-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=CY  MEMBER STATE LEGAL DETAILS FOR CZ  Actual or expected expiration date=2012-01-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=CZ     Event publication date=2012-01-31  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=CZ  MEMBER STATE LEGAL DETAILS FOR DE  Actual or expected expiration date=2026-10-10    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=DE Corresponding appl: DE602006022572    Event publication date=2011-08-04  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=2011-08-04     Event publication date=2012-07-12  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=2012-03-16     Event publication date=2017-10-04  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=2017-10-04     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=DE  MEMBER STATE LEGAL DETAILS FOR DK1937664  Actual or expected expiration date=2015-10-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=DK Corresponding appl: DK06811793  Application date in the designated or member state=2006-10-10   Application number in the designated or member state=2006DK-0811793 Corresponding cc:  Designated or member state=DK Corresponding pat: DK1937664  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2011-07-18   Publication number in the designated or member state=DK1937664T    Event publication date=2011-07-18  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=2014-10-10  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=2014-10-10     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=DK     Event publication date=2016-05-30  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   Effective date of the event=2015-10-31     Event publication date=2016-10-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=DK  MEMBER STATE LEGAL DETAILS FOR EE  Actual or expected expiration date=2012-01-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=EE     Event publication date=2012-01-31  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 EP2251336  Actual or expected expiration date=2012-07-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=EP Corresponding appl: EP10006958  Application date in the designated or member state=2006-10-10   Application number in the designated or member state=2010EP-0006958 Corresponding cc:  Designated or member state=EP Corresponding pat: EP2251336  Publication stage code in the designated or member state=A1  Publication date in the designated or member state=2010-11-17   Publication number in the designated or member state=EP2251336    Event publication date=2013-01-23  Event code=EP/STCHG  Patent status changed by the national office Corresponding cc:  Designated or member state=EP  MEMBER STATE LEGAL DETAILS FOR ES2366049  Actual or expected expiration date=2017-06-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=ES Corresponding appl: ES06811793  Application date in the designated or member state=2006-10-10   Application number in the designated or member state=2006ES-0811793T Corresponding cc:  Designated or member state=ES Corresponding pat: ES2366049  Publication stage code in the designated or member state=T3  Publication date in the designated or member state=2011-10-14   Publication number in the designated or member state=ES2366049    Event publication date=2011-10-14  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=2011-10-14     Event publication date=2014-09-11  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=2014-09-11     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=ES     Event publication date=2017-06-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=ES  MEMBER STATE LEGAL DETAILS FOR FI  Actual or expected expiration date=2011-11-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=FI     Event publication date=2011-11-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=FI  MEMBER STATE LEGAL DETAILS FOR FR  Actual or expected expiration date=2026-10-10    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=FR     Event publication date=2016-09-19  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=2016-09-19     Year of payment of annual fees=11  Corresponding cc:  Designated or member state=FR     Event publication date=2017-09-18  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=2017-09-18     Year of payment of annual fees=12  Corresponding cc:  Designated or member state=FR     Event publication date=2017-09-18  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=2017-09-18     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=2015-10-10    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=GB     Event publication date=2011-06-15  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=2014-10-08  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=2014-10-08     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=GB     Event publication date=2015-10-10  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=2015-10-10     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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=GB  MEMBER STATE LEGAL DETAILS FOR GR  Actual or expected expiration date=2016-05-06    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=GR Corresponding appl: GR20110402143    Event publication date=2011-11-22  Event code=EP/REG  Event code=GR/EP  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Ep patent validated in greece Corresponding cc:  Designated or member state=GR   Effective date of the event=2011-10-13     Event publication date=2014-09-23  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=2014-09-23     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=GR     Event publication date=2016-07-15  Event code=EP/REG  Event code=GR/ML  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Lapse due to non-payment of fees Corresponding cc:  Designated or member state=GR   Effective date of the event=2016-05-06     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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=GR  MEMBER STATE LEGAL DETAILS FOR HU  Actual or expected expiration date=2016-08-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=HU Corresponding appl: HUE012233    Event publication date=2012-02-28  Event code=EP/REG  Event code=HU/AG4A  Event indicator=Pos  Event type=Examination events  Reference to a national code Filing of the translation of the text of european patents Eurpai szabadalmak szoevege forditasanak benyujtasa Corresponding cc:  Designated or member state=HU     Event publication date=2014-09-23  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=2014-09-23     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=HU     Event publication date=2016-08-31  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=HU  MEMBER STATE LEGAL DETAILS FOR IE  Actual or expected expiration date=2012-08-01    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IE     Event publication date=2011-07-20  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=2012-08-01  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=2012-10-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=IE  MEMBER STATE LEGAL DETAILS FOR IS  Actual or expected expiration date=2012-01-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=IS     Event publication date=2012-01-31  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=IS  MEMBER STATE LEGAL DETAILS FOR IT  Actual or expected expiration date=2026-10-10    Legal state=ALIVE    Status=GRANTED   Corresponding cc:  Designated or member state=IT     Event publication date=2017-10-24  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=2017-10-24     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=2016-07-29    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LI     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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=LI  MEMBER STATE LEGAL DETAILS FOR LT  Actual or expected expiration date=2011-10-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LT     Event publication date=2011-10-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF 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=2013-05-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LU     Event publication date=2013-05-31  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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=LU  MEMBER STATE LEGAL DETAILS FOR LV  Actual or expected expiration date=2011-11-30    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=LV     Event publication date=2011-11-30  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notifications  Lapsed in a contracting state announced via postgrant inform. from nat. office to EPO LAPSE BECAUSE OF FAILURE TO SUBMIT A TRANSLATION OF THE DESCRIPTION OR TO PAY THE FEE WITHIN THE PRESCRIBED TIME-LIMIT  Corresponding cc:  Designated or member state=LV  MEMBER STATE LEGAL DETAILS FOR MC  Actual or expected expiration date=2012-05-31    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=MC     Event publication date=2012-05-31  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 NON-PAYMENT OF DUE FEES  Corresponding cc:  Designated or member state=MC  MEMBER STATE LEGAL DETAILS FOR NL  Actual or expected expiration date=2015-11-01    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=NL     Event publication date=2011-07-20  Event code=EP/REG  Event code=NL/T3  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Translation files for an european patent granted for nl, confirming art. 52 par. 1 or 6 of the patents act 1995 Voor nederland verleende europese octrooien waarvoor een vertaling is ingediend conform artikel 52 lid 1 of 6 van de ocrooiwet 1995 Corresponding cc:  Designated or member state=NL     Event publication date=2014-10-10  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=2014-10-10     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=NL     Event publication date=2016-07-06  Event code=EP/REG  Event code=NL/MM  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Lapsed because of non-payment of the annual fee [NO DESCRIPTION IN ORIGINAL LANGUAGE] Corresponding cc:  Designated or member state=NL   Effective date of the event=2015-11-01     Event publication date=2016-08-31  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=NL  MEMBER STATE LEGAL DETAILS FOR PL  Actual or expected expiration date=2017-02-28    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=PL     Event publication date=2011-11-30  Event code=EP/REG  Event code=PL/T3  Event indicator=Pos  Event type=Event indicating In Force  Reference to a national code Translation of ep patent Tlumaczenia patentow europejskich Corresponding cc:  Designated or member state=PL     Event publication date=2014-09-16  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=2014-09-16     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=PL     Event publication date=2017-02-28  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=PL  MEMBER STATE LEGAL DETAILS FOR PT  Actual or expected expiration date=2016-04-11    Legal state=DEAD    Status=LAPSED   Corresponding cc:  Designated or member state=PT     Event publication date=2011-07-07  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=2011-06-29  AVAILABILITY OF NATIONAL TRANSLATION     Event publication date=2014-10-10  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=2014-10-10     Year of payment of annual fees=9  Corresponding cc:  Designated or member state=PT     Event publication date=2016-04-18  Event code=EP/REG  Event code=PT/MM4A  Event indicator=Neg  Event type=Event indicating Not In Force  Reference to a national code Annulment/lapse due to non-payment of fees, searched and examined patent Caducada por falta de pagamento de taxas, patente de invencao pesquisada e examinado Corresponding cc:  Designated or member state=PT   Effective date of the event=2016-04-11  LAPSE DUE TO NON-PAYMENT OF FEES     Event publication date=2016-08-31  Event code=EP/PG25  Event indicator=Neg  Event type=Event indicating Not In Force  Event type=Payment or non-payment notification(...)
专利类型码
A1B1
国别省市代码
若您需要申请原文,请登录。

最新评论

暂无评论。

登录后可以发表评论

意见反馈
返回顶部