IP Library › Granted Patent US 9,120,823
Granted Patent B2
US 9,120,823 · App. 14/669,492 · Granted Sep 1, 2015

Fused heterocyclic compound and use thereof for pest control

Inventors: Masaki Takahashi (Takarazuka, JP); Takamasa Tanabe (Takarazuka, JP); Mai Ito (Takarazuka, JP); Yoshihiko Nokura (Takarazuka, JP)
Assignee: Sumitomo Chemical Company, Limited
C07D513/04A01N43/52A01N43/90C07D401/04C07D471/04C07D498/04
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Quick Facts
Patent No.
US 9,120,823
App. No.
14/669,492
Granted
Sep 1, 2015
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 (14)

1. A compound represented by the formula (M3-1):

or an N-oxide thereof;

wherein

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

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

R 1a represents a C1-C6 alkyl group optionally substituted by one or more atoms or groups selected from the group consisting of a halogen atom and a cyclopropyl group (wherein the cyclopropyl group is optionally substituted by one or more halogen atoms or one or more C1-C3 alkyl groups), a C2-C6 alkenyl group optionally substituted by one or more halogen atoms or a C2-C6 alkynyl group optionally substituted by one or more halogen atoms,

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, —OR 22a (wherein R 22a represents a C1-C6 alkyl group optionally substituted by one or more halogen atoms), —S(O)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),

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, and

n represents 0, 1 or 2.

2. The compound according to claim 1 , wherein A 1a in the formula (M3-1) is NR 7a .

3. The compound according to claim 1 , wherein A 1a in the formula (M3-1) is an oxygen atom.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Mar 27, 2015
From: TAKAHASHI, MASAKI; TANABE, TAKAMASA; ITO, MAI; NOKURA, YOSHIHIKO
To: SUMITOMO CHEMICAL COMPANY, LIMITED
Reel/Frame 035270/0141 →
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 (2)
Division 14234717
Related Publication 20150197532A1 · Jul 16, 2015