IP Library Granted Patent US 8,946,492
Granted Patent B2
US 8,946,492 · App. 13/850,067 · Granted Feb 3, 2015

Isoxazoline-substituted benzamide compound and pesticide

Inventors: Takeshi Mita (Funabashi, JP); Takamasa Kikuchi (Funabashi, JP); Takashi Mizukoshi (Chiba, JP); Manabu Yaosaka (Funabashi, JP); Mitsuaki Komoda (Funabashi, JP)
Assignee: Nissan Chemical Industries, Ltd.
C07D413/14C07C25/13C07C25/24C07C25/02C07C25/06C07C25/08A01N43/80C07C43/1742C07C43/1745C07C205/11C07C205/12C07C211/52C07C251/48C07C255/29C07C255/50C07C255/60C07C281/02C07C323/09C07D261/16C07D413/04C07D413/06C07D413/12C07D417/06C07D417/12C07F7/0812C07D261/04
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Quick Facts
Patent No.
US 8,946,492
App. No.
13/850,067
Granted
Feb 3, 2015
Kind
B2
Abstract

A substituted alkenylbenzene compound of formula (4): wherein X 1 is selected from the group consisting of a halogen atom, —SF 5 , C 1 -C 6 haloalkyl, hydroxy C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy C 1 -C 6 haloalkyl, C 3 -C 8 halocycloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 3 haloalkoxy C 1 -C 3 haloalkoxy, C 1 -C 6 haloalkylthio, C 1 -C 6 haloalkylsulfinyl and C 1 -C 6 haloalkylsulfonyl; X 3 is selected from the group consisting of a hydrogen atom, halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy and C 1 -C 6 alkylthio; X 4 is selected from the group consisting of a hydrogen atom, halogen atom, cyano, C 1 -C 4 alkyl, C 1 -C 4 alkoxy and C 1 -C 4 haloalkoxy; R 3 is —C(R 3a )(R 3b )R 3c , where R 3a and R 3b independently of each other are a halogen atom, or R 3a and R 3b together form 3 - to 6 -membered ring together with the carbon atom bonding them by forming a C 2 -C 5 haloalkylene chain, and R 3c is selected from the group consisting of a hydrogen atom, halogen atom, C 1 -C 5 alkyl, C 1 -C 5 haloalkyl, C 1 -C 4 haloalkoxy and C 1 -C 4 haloalkylthio, with a proviso that in case where X 1 is a fluorine atom, chlorine atom or trifluoromethyl, and both X 2 and X 3 are a hydrogen atom, in case where both X 1 and X 2 are fluorine atom and X 3 is a hydrogen atom, and in case where both X 1 and X 2 are trifluoromethyl and X 3 is a hydrogen atom, R 3c is a hydrogen atom, chlorine atom, bromine atom, iodine atom, C 1 -C 5 alkyl, C 1 -C 5 haloalkyl, C 1 -C 4 haloalkoxy or C 1 -C 4 haloalkylthio.

Claims (14)

1. A substituted alkenylbenzene compound of formula (4):

wherein:

X 1 is selected from the group consisting of a halogen atom, —SF 5 , C 1 -C 6 haloalkyl, hydroxyl C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy C 1 -C 6 haloalkyl, C 3 -C 8 halocycloalkyl, C 1 -C 6 haloalkoxy, C 1 -C 3 haloalkoxy C 1 -C 3 haloalkoxy, C 1 -C 6 haloalkylthio, C 1 -C 6 haloalkylsulfinyl and C 1 -C 6 haloalkylsulfonyl;

X 3 is selected from the group consisting of a hydrogen atom, halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl, C 1 -C 6 alkoxy and C 1 -C 6 alkylthio; and

X 4 is selected from the group consisting of a hydrogen atom, halogen atom, cyano and C 1 -C 4 haloalkoxy;

R 3 is —C(R 3a )(R 3b )R 3c , where

R 3a and R 3b independently of each other are a halogen atom, or R 3a and R 3b together from 3- to 6-membered ring together with the carbon atom bonding them by forming a C 2 -C 5 haloalkylene chain, and

R 3c is selected from the group consisting of a hydrogen atom, halogen atom, C 1 -C 5 alkyl, C 1 -C 5 haloalkyl, C 1 -C 4 haloalkoxy and C 1 -C 4 haloalkylthio, with a proviso that in case where X 1 is a fluorine atom, chlorine atom or trifluoromethyl, and both X 3 and X 4 are a hydrogen atom, in case where both X 1 and X 3 are fluorine atom and X 4 is a hydrogen atom, and in case where both X 1 and X 3 are trifluoromethyl and X 4 is a hydrogen atom, R 3c is a hydrogen atom, chlorine atom, bromine atom, iodine atom, C 1 -C 5 alkyl, C 1 -C 5 haloalkyl, C 1 -C 4 haloalkoxy or C 1 -C 4 haloalkylthio.

2. The substituted alkenylbenzene compound of formula (4) according to claim 1 , wherein:

X 1 is selected from the group consisting of a halogen atom, —SF 5 , C 1 -C 6 haloalkyl, C 1 -C 6 haloalkoxy and C 1 -C 6 haloalkylthio;

X 3 is selected from the group consisting of a hydrogen atom, halogen atom, cyano, nitro, C 1 -C 6 alkyl, C 1 -C 6 haloalkyl and C 1 -C 6 alkoxy;

X 4 is a hydrogen atom or halogen atom;

R 3a and R 3b are each a fluorine atom;

R 3c is selected from the group consisting of a hydrogen atom, fluorine atom, chlorine atom, bromine atom and trifluoromethyl, with a proviso that in case where X 1 is a fluorine atom, chlorine atom or trifluoromethyl and both X 3 and X 4 are a hydrogen atom, in case where both X 1 and X 3 are a fluorine atom and X 4 is a hydrogen atom, and in case where both X 1 and X 3 are trifluoromethyl and X 4 is a hydrogen atom, R 3c is a hydrogen atom, chlorine atom, bromine atom or trifluoromethyl.

Assignments (2)
CHANGE OF NAME Recorded Sep 21, 2018
From: NISSAN CHEMICAL INDUSTRIES, LTD.
To: NISSAN CHEMICAL CORPORATION
Reel/Frame 047128/0788 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jul 16, 2013
From: MITA, TAKESHI; KIKUCHI, TAKAMASA; MIZUKOSHI, TAKASHI; YAOSAKA, MANABU; KOMODA, MITSUAKI
To: NISSAN CHEMICAL INDUSTRIES, LTD.
Reel/Frame 030807/0905 →
Priority Claims (2)
JP 2004-061749 · Mar 5, 2004 · national
JP 2004-200119 · Jul 7, 2004 · national
Continuity (5)
Division 13166294 · Jun 22, 2011
Division 12509859 · Jul 27, 2009
Division 11514921 · Sep 5, 2006
Continuation In Part PCTJP2005004268 · Mar 4, 2005
Related Publication 20130296559A1 · Nov 7, 2013