IP Library › Granted Patent US 9,353,110
Granted Patent B2
US 9,353,110 · App. 14/801,978 · Granted May 31, 2016

Fused heterocyclic compound

Inventors: Masaki Takahashi (Takarasuka, JP); Takamasa Tanabe (Takarazuka, JP); Mai Ito (Takarazuka, JP); Yoshihiko Nokura (Takarasuka, JP)
Assignee: Sumitomo Chemical Company, Limited
C07D471/04A01N43/52A01N43/76A01N43/78A01N43/90C07D401/04C07D413/04C07D417/04C07D495/04C07D498/04C07D513/04
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Quick Facts
Patent No.
US 9,353,110
App. No.
14/801,978
Granted
May 31, 2016
Kind
B2
Abstract

There is provided a compound having an excellent controlling effect on pests represented by the formula (1): wherein, A 1 represents —NR 7 —, etc., A 2 represents a nitrogen atom, etc., A 3 represents a nitrogen atom, etc., R 1 represents a C1-C6 chain hydrocarbon group optionally substituted by one or more atoms or groups selected from Group X, etc., R 2 , R 3 and R 4 are the same or different and each represents a C1-C6 chain hydrocarbon group optionally substituted by one or more halogen atoms, etc., R 5 and R 6 are the same or different and each represents a C1-C6 chain hydrocarbon group optionally substituted by one or more atoms or groups selected from Group X, etc., R 7 represents a C1-C6 chain hydrocarbon group optionally substituted by one or more atoms or groups selected from Group W, etc., n represents 0, 1 or 2, or an N-oxide thereof.

Claims (12)

1. A compound represented by the formula (M6-1):

wherein

V 2 represents a halogen atom,

A 1a represents —NR 7a —, an oxygen atom or a sulfur atom,

A 3a represents a nitrogen atom or ═CR 9a —,

R 2a and R 4a are the same or different and each represents a halogen atom or a hydrogen atom,

R 3a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, a C2-C6 alkenyl group optionally substituted by one or more halogen atoms, a C2-C6 alkynyl group optionally substituted by one or more halogen atoms, 5- or 6-membered aromatic heterocyclic group (wherein the 5- or 6-membered aromatic heterocyclic group is optionally substituted by one or more atoms or groups selected from the group consisting of a halogen atom, a C1-C3 alkyl group optionally substituted by one or more halogen atoms, and a C1-C3 alkoxy group optionally substituted by one or more halogen atoms), —OR 20a (wherein R 20a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms), S(O) m R 21a (wherein R 21a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, m represents 0, 1 or 2), a cyano group, a nitro group, a halogen atom or a hydrogen atom,

R 5a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, —S(O) m,, R 23a (wherein R 23a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, m represents 0, 1 or 2), —SF 5 or a halogen atom,

R 7a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, a C3-C6 alkenyl group optionally substituted by one or more halogen atoms, a C3-C6 alkynyl group optionally substituted by one or more halogen atoms, or a C1-C6 alkyl group substituted by one 5- or 6-membered aromatic heterocyclic group, (wherein the 5- or 6-membered aromatic heterocyclic group is optionally substituted by one or more atoms or groups selected from the group consisting of a halogen atom, a C1-C3 alkyl group optionally substituted by one or more halogen atoms, and a C1-C3 alkoxy group optionally substituted by one or more halogen atoms), and

R 9a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, —OR 24a (wherein R 24a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms), —S(O) m R 25a (wherein R 25a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms, m represents 0, 1 or 2), a halogen atom or a hydrogen atom,

or an N-oxide thereof.

2. The compound according to claim 1 , wherein A 1a is —NR 7a — in the formula (M6-1).

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Aug 11, 2015
From: TAKAHASHI, MASAKI; TANABE, TAKAMASA; ITO, MAI; NOKURA, YOSHIHIKO
To: SUMITOMO CHEMICAL COMPANY, LIMITED
Reel/Frame 036299/0570 →
Priority Claims (3)
JP 2011-170833 · Aug 4, 2011 · national
JP 2012-079323 · Mar 30, 2012 · national
JP 2012-122837 · May 30, 2012 · national
Continuity (3)
Division 14669492 · Mar 26, 2015
Division 14234717
Related Publication 20160009715A1 · Jan 14, 2016