IP Library › Granted Patent US 8,853,238
Granted Patent B2
US 8,853,238 · App. 13/996,697 · Granted Oct 7, 2014

Fused heterocyclic compound and use thereof for pest control

Inventors: Hayato Takyo (Tokyo, JP); Masaki Takahashi (Takarazuka, JP); Takamasa Tanabe (Takarazuka, JP); Yoshihiko Nokura (Takarazuka, JP); Mai Ito (Takarazuka, JP); Atsushi Iwata (Tokyo, JP)
Assignee: Sumitomo Chemical Company, Limited
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Quick Facts
Patent No.
US 8,853,238
App. No.
13/996,697
Granted
Oct 7, 2014
Kind
B2
Abstract

A fused heterocyclic compound the formula (1): wherein A 1 represents —NR 8 —, and the like; A 2 represents a nitrogen atom, and the like; A 3 represents a nitrogen atom, and the like; R 1 represents a C1-C6 chain hydrocarbon group optionally having one or more atoms or groups selected from Group X, and the like; R 2 , R 3 , R 4 , and R 5 are same or different and represent independently a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, and the like; R 6 and R 7 are same or different and represent independently a C1-C6 chain hydrocarbon group optionally having one or more atoms or groups selected from Group X, and the like; R 8 represents a C1-C6 chain hydrocarbon group optionally having one or more atoms or groups selected from Group W, and the like; n represents 0, 1 or 2. The compound has an excellent activity of controlling pests.

Claims (40)

1. A fused heterocyclic compound of the formula (I):

wherein:

A 1 represents —NR 8 —, an oxygen atom, or a sulfur atom;

A 2 represents ═CR 9 —;

A 3 represents a nitrogen atom;

R 1 represents a C1-C6 chain hydrocarbon group optionally having one or more atoms or groups selected from Group X, or a C3-C6 alicyclic hydrocarbon group optionally having one or more atoms or groups selected from Group Y;

R 2 , R 3 , R 4 , and R 5 are same or different and independently represent a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, a phenyl group optionally having one or more atoms or groups selected from Group Z, a 5-membered heterocyclic group optionally having one or more atoms or groups selected from Group Z, a 6-membered heterocyclic group optionally having one or more atoms or groups selected from Group Z, —OR 11 , —S(O) m R 11 , —NR 11 R 12 , —CO 2 R 11 , —C(O)R 11 , a cyano group, a nitro group, a halogen atom, —SF 5 , or a hydrogen atom, provided that at least two of R 2 , R 3 , R 4 , and R 5 represent a hydrogen atom;

R 6 and R 7 are same or different and independently represent a C1-C6 chain hydrocarbon group optionally having one or more atoms or groups selected from Group X, a phenyl group optionally having one or more atoms or groups selected from Group Z, a 5-membered heterocyclic group optionally having one or more atoms or groups selected from Group Z, a 6-membered heterocyclic group optionally having one or more atoms or groups selected from Group Z, —OR 11 , —S(O) m R 11 , —S(O) 2 NR 11 R 12 , —NR 11 R 12 , —NR 11 —CO 2 R 12 , —NR 11 C(O)R 12 , —CO 2 R 11 , —C(O)R 11 , a cyano group, a nitro group, a halogen atom, —SF 5 , or a hydrogen atom;

R 8 represents a C1-C6 chain hydrocarbon group optionally having one or more atoms or groups selected from Group W, —CO 2 R 11 , —C(O)R 11 , or a C3-C6 alicyclic hydrocarbon group optionally having one or more atoms or groups selected from Group Y;

R 9 represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, —OR 11 , —S(O) m R 11 , —NR 11 R 12 , —CO 2 R 11 , —C(O)R 11 , a cyano group, a nitro group, a halogen atom, or a hydrogen atom;

R 11 and R 12 are same or different and independently represent a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, or a hydrogen atom; and

m represents 0, 1, or 2; and n represents 0, 1, or 2;

(except in cases as follows: both R 6 and R 7 are a hydrogen atom; and in —S(O) m R 11 , when m is 1 or 2, R 11 is a hydrogen atom)

the Group X consists of a C1-C6 alkoxy group optionally having one or more halogen atoms, a C2-C6 alkenyloxy group optionally having one or more halogen atoms, a C2-C6 alkynyloxy group optionally having one or more halogen atoms, a C1-C6 alkylsulfanyl group optionally having one or more halogen atoms, a C1-C6 alkylsulfinyl group optionally having one or more halogen atoms, a C1-C6 alkylsulfonyl group optionally having one or more halogen atoms, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group optionally having one or more halogen atoms, a C3-C6 cycloalkyl group optionally having one or more halogen atoms, a cyano group, a hydroxy group, and a halogen atom;

the Group Y consists of a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, a C1-C6 alkoxy group optionally having one or more halogen atoms, a C2-C6 alkenyloxy group optionally having one or more halogen atoms, a C2-C6 alkynyloxy group optionally having one or more halogen atoms, a hydroxy group, and a halogen atom;

the Group Z consists of a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, a C1-C6 alkoxy group optionally having one or more halogen atoms, a C1-C6 alkylsulfanyl group optionally having one or more halogen atoms, a C1-C6 alkylsulfinyl group optionally having one or more halogen atoms, a C1-C6 alkylsulfonyl group optionally having one or more halogen atoms, a C2-C6 alkylcarbonyl group optionally having one or more halogen atoms, a C2-C6 alkoxycarbonyl group optionally having one or more halogen atoms, a C1-C6 alkylamino group optionally having one or more halogen atoms, a C2-C8 dialkylamino group optionally having one or more halogen atoms, a halogen atom, a cyano group, and a nitro group; and

the Group W consists of a C1-C6 alkoxy group optionally having one or more halogen atoms, a C2-C6 alkenyloxy group optionally having one or more halogen atoms, a C2-C6 alkynyloxy group optionally having one or more halogen atoms, a C1-C6 alkylsulfanyl group optionally having one or more halogen atoms, a C1-C6 alkylsulfinyl group optionally having one or more halogen atoms, a C1-C6 alkylsulfonyl group optionally having one or more halogen atoms, a C2-C6 alkylcarbonyl group, a C2-C6 alkoxycarbonyl group, a C3-C6 cycloalkyl group, a halogen atom, a cyano group, and a hydroxy group.

2. The fused heterocyclic compound according to claim 1 , wherein R 6 and R 7 are same or different and are independently a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, —OR 11 , —S(O) m R 11 , —NR 11 R 12 , a cyano group, a nitro group, a halogen atom, or a hydrogen atom.

3. The fused heterocyclic compound according to claim 1 , wherein R 6 and R 7 are same or different and are independently a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, —OR 11 , —S(O) m R 11 , a halogen atom, or a hydrogen atom.

4. The fused heterocyclic compound according to claim 1 , wherein A 2 is ═CH—.

5. The fused heterocyclic compound according to claim 1 , wherein R 2 , R 4 , and R 5 are same or different and are independently a hydrogen atom or a halogen atom, and R 3 is a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, —OR 11 , a halogen atom, or a hydrogen atom.

6. The fused heterocyclic compound according to claim 1 , wherein A 1 is —NR 8 —, and R 8 is a C1-C6 chain hydrocarbon group having one C1-C6 alkoxy group optionally having one or more halogen atoms, a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, or a cyclopropyl group.

7. The fused heterocyclic compound according to claim 1 , wherein A 1 is —NR 8 —, and R 8 is a methyl group, an ethyl group, a methoxymethyl group, or an ethoxymethyl group.

8. The fused heterocyclic compound according to claim 1 , wherein A 1 is an oxygen atom.

9. The fused heterocyclic compound according to claim 1 , wherein A 1 is a sulfur atom.

10. The fused heterocyclic compound according to claim 1 which is represented by the formula (1-1):

wherein:

A 1a represents —NR 8a — or a sulfur atom;

A 3a represents a nitrogen atom;

R 1a represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms;

R 2a , R 4a , and R 5a are same or different and independently represent a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, a halogen atom, or a hydrogen atom;

R 3a represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, —OR 11a , a halogen atom, or a hydrogen atom;

R 6a represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms, —OR 11a , —S(O) m R 11a , a bromine atom, or an iodine atom;

R 8a represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms;

R 11a represents a C1-C6 chain hydrocarbon group optionally having one or more halogen atoms; and

m represents 0, 1, or 2, and n represents 0, 1, or 2;

provided that in —S(O) m R 11 , when m is 1 or 2, R 11 is not a hydrogen atom.

11. The fused heterocyclic compound according to claim 10 , wherein A 1a is —NR 8a — or a sulfur atom, R 8a is a methyl group, A 3a is a nitrogen atom, R 1a is an ethyl group, R 2a , R 4a , and R 5a are same or different and are independently a halogen atom or a hydrogen atom, R 3a is a trifluoromethyl group, a halogen atom, or a hydrogen atom, and R 6a is a C1-C3 alkyl group having one or more fluorine atoms, a C1-C3 alkoxy group having one or more fluorine atoms, a C1-C3 alkylsulfanyl group having one or more fluorine atoms, a C1-C3 alkylsulfinyl group having one or more fluorine atoms, or a C1-C3 alkylsulfonyl group having one or more fluorine atoms.

12. A pest controlling composition which comprises the fused heterocyclic compound according to claim 1 and an inert carrier.

13. A method of controlling pests which comprises applying an effective amount of the fused heterocyclic compound according to claim 1 to pests or habitats of pests.

Assignments (1)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Sep 9, 2013
From: TAKYO, HAYATO; TAKAHASHI, MASAKI; TANABE, TAKAMASA; NOKURA, YOSHIHIKO; ITO, MAI; IWATA, ATSUSHI
To: SUMITOMO CHEMICAL COMPANY, LIMITED
Reel/Frame 031160/0904 →
Priority Claims (3)
JP 2010-287412 · Dec 24, 2010 · national
JP 2011-166768 · Jul 29, 2011 · national
JP 2011-263374 · Dec 1, 2011 · national
Continuity (1)
Related Publication 20140018373A1 · Jan 16, 2014