IP Library Granted Patent US 9,686,990
Granted Patent B2
US 9,686,990 · App. 14/859,410 · Granted Jun 27, 2017

Spiroindolinepiperidine derivatives

Inventors: David John Hughes (Bracknell, GB); Paul Anthony Worthington (Bracknell, GB); Charles Adam Russell (Bracknell, GB); Eric Daniel Clarke (Bracknell, GB); James Edward Peace (Bracknell, GB); Mark Richard Ashton (Abington, GB); Thomas Stephen Coulter (Abington, GB); Richard Spurring Roberts (Barcelona, ES); Louis-Pierre Molleyres (Basel, CH); Fredrik Cederbaum (Stein, CH); Jerome Cassayre (Stein, CH); Peter Maienfisch (Stein, CH)
Assignee: Syngenta Participations AG
A01N43/90A01N47/34A01N47/38C07D211/70C07D211/76C07D471/10C07D491/10C07B2200/11
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Quick Facts
Patent No.
US 9,686,990
App. No.
14/859,410
Granted
Jun 27, 2017
Kind
B2
Abstract

Insecticidal, acaricidal, nematicidal or molluscicidal compounds of formula (I) wherein Y is a single bond, C═O, C═S or S(O) q where q is 0, 1 or 2; and R 1 , R 2 , R 3 , R 4 , R 8 , R 9 are R 10 are as defined in the claims or salts or N-oxides thereof, processes for preparing them and compositions containing them.

Claims (13)

1. A compound of formula IN

wherein

Y is C═O;

R 1 is C 1-6 alkyl, C 1-6 haloalkyl, heteroaryl(C 1-3 )alkyl (wherein the heteroaryl group may be optionally substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino and the heteroaryl group is a pyridine, pyrimidine, pyrazine or pyridazine ring), heteroaryl (optionally substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino and where the heteroaryl group is a pyridine, pyrimidine, pyrazine or pyridazine ring), C 1-6 alkoxy or heterocyclyl (optionally substituted by halo, cyano, C 1-3 alkyl, C 1-3 haloalkyl, or C 1-3 alkoxy);

each R 4 is independently fluoro, chloro, bromo, cyano, C 1-4 alkyl, C 1-4 haloalkyl, C 1-4 cyanoalkyl or C 1-3 alkoxy(C 1-3 )alkyl; n is 0, 1 or 2;

R 8 is phenyl(C 2-4 )alkenyl (wherein the phenyl group is optionally substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino, dialkylamino or C 1-3 alkoxycarbonyl) or phenyl(C 2-4 )alkynyl (wherein the phenyl group is optionally substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino, dialkylamino or C 1-3 alkoxycarbonyl); or

R 8 is —C(R 51 )(R 52 )—[CR 53 ═CR 54 ]z-R 55 where z is 1, R 51 and R 52 are each independently H, halo or C 1-2 alkyl, R 53 and R 54 are each independently H, halogen, C 1-4 alkyl or C 1-4 haloalkyl and R 55 is phenyl substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino or heteroaryl substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino; and

R 2 R 3 R 9 and R 10 are all hydrogen; and salts or N-oxides thereof.

2. An insecticidal, acaricidal or nematicidal composition comprising an insecticidally, acaricidally or nematicidally effective amount of a compound of formula IN as defined in claim 1 .

3. A compound according to claim 1 wherein R 1 is pyridyl (optionally substituted by halo, C 1-3 alkyl or C 1-3 haloalkyl) or C 1-6 alkoxy.

4. A compound according to claim 1 wherein each R 4 is independently fluoro, chloro, bromo, C 1-4 alkyl or C 1-4 haloalkyl; n is 1 or 2.

5. A compound according to claim 1 wherein R 8 is —C(R 51 )(R 52 )_[CR 53 ═CR 54 ]z-R 55 where z is 1, R 51 and R 52 are each independently H, halo or C 1-2 alkyl, R 53 and R 54 are each independently H, halogen, C 1-4 alkyl or C 1-4 haloalkyl and R 55 is phenyl substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino or heteroaryl substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino.

6. A compound according to claim 1 wherein R 1 is pyridyl (optionally substituted by halo, C 1-3 alkyl or C 1-3 haloalkyl) or C 1-6 alkoxy; each R 4 is independently fluoro, chloro, bromo, C 1-4 alkyl or C 1-4 haloalkyl; n is 1 or 2; and R 8 is —C(R 51 )(R 52 )—[CR 53 ═CR 54 ]z-R 55 where z is 1, R 51 and R 52 are each independently H, halo or C 1-2 alkyl, R 53 and R 54 are each independently H, halogen, C 1-4 alkyl or C 1-4 haloalkyl and R 55 is phenyl substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino or heteroaryl substituted by halogen, C 1-4 alkyl, C 1-4 alkoxy, C 1-4 haloalkyl, C 1-4 haloalkoxy, CN, NO 2 , aryl, heteroaryl, amino or dialkylamino; and salts or N-oxides thereof.

Priority Claims (1)
GB 0213715.6 · Jun 14, 2002 · national
Continuity (3)
Division 13234793 · Sep 16, 2011
Division 10517957
Related Publication 20160007608A1 · Jan 14, 2016