IP Library Granted Patent US 9,920,046
Granted Patent B2
US 9,920,046 · App. 15/207,764 · Granted Mar 20, 2018

Oxime-substituted amide compound and pest control agent

Inventors: Motoyoshi Iwasa (Funabashi, JP); Keisuke Tsuji (Funabashi, JP); Mitsutaka Tomizawa (Funabashi, JP); Takeshi Mita (Funabashi, JP); Hidehito Kuwahara (Shiraoka, JP); Miho Asahi (Shiraoka, JP); Hotaka Imanaka (Shiraoka, JP)
Assignee: Nissan Chemical Industries, Ltd.
C07D417/12A01N37/18A01N37/20A01N37/34A01N41/10A01N41/12A01N43/10A01N43/40A01N43/56A01N43/60A01N43/713A01N43/76A01N43/78A01N43/80A01N43/84A01N47/12A01N55/00C07C251/48C07C251/52C07C255/64C07C317/32C07C321/28C07D213/42C07D213/53C07D213/61C07D213/65C07D213/82C07D241/24C07D333/38C07D401/12C07D405/12C07D407/12C07D409/12C07D413/12C07F7/0814
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Quick Facts
Patent No.
US 9,920,046
App. No.
15/207,764
Granted
Mar 20, 2018
Kind
B2
Abstract

To provide a novel pesticide, especially a fungicide and a nematocide. An oxime-substituted amide compound represented by the formula (I) or its salt, and a pesticide containing it: wherein G 1 is a structure represented by G 1 -1 or the like, G 2 is a structure represented by G 2 -2 or the like: W is an oxygen atom or the like, X 1 is a halogen atom, methyl, trifluoromethyl or the like, each of X 2 , X 3 , X 4 and X 5 is independently a hydrogen atom, a halogen atom or the like, each of Y 1 and Y 3 is independently a halogen atom, cyano, methyl, trifluoromethyl, C 2 -C 6 alkynyl or the like, each of Y 2 and Y 4 is independently a hydrogen atom, a halogen atom or the like, R 1 is C 1 -C 6 alkyl, C 1 -C 4 haloalkyl, (C 1 -C 4 )alkyl substituted with R 18 , C 3 -C 6 cycloalkyl, C 3 -C 6 alkenyl or the like, each of R 2 and R 3 is independently a hydrogen atom, methyl or the like, R 4 is a hydrogen atom or the like, R 18 is C 3 -C 6 cycloalkyl, phenyl, phenyl substituted with (Z) m or the like, Z is a halogen atom or the like, and m is an integer of 1, 2 or 3.

Claims (25)

1. A compound, which is represented by formula (IVa):

wherein:

G 1 is a structure represented by any one of G 1 -1, G 1 -2 and G 1 -3:

X 1 is a halogen atom, nitro, methyl, difluoromethyl or trifluoromethyl;

X 2 , X 3 and X 5 are hydrogen atoms;

X 4 is a hydrogen atom, and when G 1 is G 1 -1, X 4 is optionally a halogen atom;

Y 1 is a halogen atom;

Y 2 is a hydrogen atom, a halogen atom or cyano;

Y 3 is a halogen atom, cyano, methyl, trifluoromethyl, C 1 -C 4 alkoxy, C 1 -C 4 haloalkoxy, -C(R 10 )═NOR 11 , C 2 -C 4 alkenyl, C 2 -C 6 alkynyl, (C 2 -C 6 )alkynyl substituted with R 6 , D-3 or D-7;

Y 4 is a hydrogen atom or a halogen atom;

R 2 is a hydrogen atom or methyl;

R 6 is a halogen atom, C 3 -C 6 cycloalkyl, —OH, trimethylsilyl or phenyl;

R 10 is methyl; and

R 11 is methyl or ethyl.

2. The compound according to claim 1 , wherein G 1 is G 1 -1.

3. The compound according to claim 1 , wherein G 1 is G 1 -2.

4. The compound according to claim 1 , wherein G 1 is G 1 -3.

5. The compound according to claim 1 , wherein the compound is:

6. The compound according to claim 1 , wherein the compound is:

7. The compound according to claim 1 , wherein the compound is:

8. The compound according to claim 1 , wherein the compound is:

9. The compound according to claim 1 , wherein the compound is:

10. The compound according to claim 1 , wherein the compound is:

11. The compound according to claim 1 , wherein the compound is:

12. The compound according to claim 1 , wherein the compound is:

Assignments (1)
CHANGE OF NAME AND ADDRESS Recorded Oct 19, 2018
From: NISSAN CHEMICAL INDUSTREIS, LTD.
To: NISSAN CHEMICAL CORPORATION
Reel/Frame 047271/0151 →
Priority Claims (3)
JP 2012-156398 · Jul 12, 2012 · national
JP 2013-019666 · Feb 4, 2013 · national
JP 2013-103989 · May 16, 2013 · national
Continuity (2)
Continuation 14414173
Related Publication 20160318919A1 · Nov 3, 2016