Processes for the preparation of pesticidal compounds

Patent metadata

Field	Value
Publication number	US-9260396-B2
Application number	US-201514718621-A
Country	US
Kind code	B2
Filing date	May 21, 2015
Priority date	Oct 17, 2013
Publication date	Feb 16, 2016
Grant date	Feb 16, 2016

Abstract

The present application provides processes for making pesticidal compounds and compounds useful both as pesticides and in the making of pesticidal compounds.

First claim

What is claimed is:

1. A process comprising:
 (a) halogenating and reducing 4-nitropyrazole

with concentrated hydrochloric acid at a temperature between about 10° C. and about 20° C. with between about 1 and about 4 equivalents of triethylsilane and about 1 to 10 weight percent palladium on alumina to yield 3-chloro-1H-pyrazol-4-amine hydrochloride (1a)

 (b) reacting (1a) with activated carbonyl thioether X 1 C(═O)C 1 -C 4 -alkyl-S—R 1 wherein X 1 is selected from Cl, OC(═O)C 1 -C 4 alkyl, or a group that forms an activated carboxylic acid and R 1 is selected form the group consisting of C 1 -C 4 haloalkyl and C 1 -C 4 alkyl-C 3 -C 6 halocycloalkyl to yield thioether

 (c) heteroarylation of (3a) with a halopyridine in the presence of a copper salt, an amine, and a base to yield thioether (3b)

 (d) alkylating a thioether (3b) with R 2 —X 2 in the presence of a base
wherein R 2 is selected from the group consisting of C 1 -C 4 -alkyl and C 2 -C 4 -alkynyl, and
wherein X 2 is a leaving group, to yield thioether (3c)

2. A The process according to claim 1 , wherein R 1 is CH 2 CH 2 CF 3 , and the activated carbonyl thioether X 1 C(═O)C 1 -C 4 -alkyl-S—R 1 , wherein X 1 is selected from Cl, OC(═O)C 1 -C 4 alkyl, or a group that forms an activated carboxylic acid, is prepared from

which has been prepared by the photochemical free-radical coupling of 3-mercaptopropionic acid and esters thereof with 3,3,3-trifluoropropene in the presence of 2,2-dimethoxy-2-phenylacetophenone initiator and long wavelength UV light in an inert organic solvent.

3. A The process according to claim 1 , wherein R 1 is CH 2 CH 2 CF 3 and the activated carbonyl thioether X 1 C(═O)C 1 -C 4 -alkyl-S—R 1 wherein X 1 is selected from Cl, OC(═O)C 1 -C 4 alkyl, or a group that forms an activated carboxylic acid is prepared from

which has been prepared by the low temperature free-radical initiated coupling of 3-mercaptopropionic acid with 3,3,3-trifluoropropene in the presence of 2,2′-azobis(4-methoxy-2,4-dimethyl) valeronitrile (V-70) initiator at temperatures of about −50° C. to about 40° C. in an inert organic solvent.

4. A The process according to claim 1 , wherein thioether (3c)

is prepared by alkylating thioether (3b) with R 2 —X 2

wherein R 2 is selected from the group consisting of C 1 -C 4 -alkyl and C 2 -C 4 -alkynyl, wherein X 2 is a leaving group, in the presence of a base, in the presence of a polar aprotic solvent, and in the presence of an iodide additive.

5. The process of claim 1 , wherein the halogenating and reducing is conducted in a polar protic solvent.

6. The process of claim 5 , wherein the polar protic solvent is methanol or ethanol.

7. The process of claim 1 , wherein the triethylsilane is used in an amount of about 2.5 equivalents to about 3.5 equivalents.

8. The process of claim 1 , wherein R 1 is CH 2 CH 2 CF 3 or CH 2 (2,2-difluorocyclopropyl).

9. The process of claim 1 , wherein X 1 is Cl or OC(═O)C 1 -C 4 alkyl.

10. The process of claim 1 , wherein step (b) is carried out in the presence of a base.

11. The process of claim 10 , wherein the base is sodium bicarbonate.

12. The process of claim 1 , wherein step (b) is carried out at a temperature of from about −10° C. to about 40° C.

13. The process of claim 1 , wherein the copper salt in step (c) is selected from the group consisting of copper(I) chloride, copper(II) chloride, and copper(I) iodide.

14. The process of claim 1 , wherein the base in step (c) is potassium phosphate or potassium carbonate.

15. The process of claim 1 , wherein the amine in step (c) is N,N′-dimethylethane-1,2-diamine.

16. The process of claim 1 , wherein step (c) is carried out in a polar solvent.

17. The process of claim 16 , wherein the polar solvent is acetonitrile, dioxane, or N,N-dimethylformamide.

18. The process of claim 1 , wherein step (c) is carried out at a temperature of from about 50° C. and about 110° C.

19. The process of claim 1 , wherein X 2 is halo, mesylate, or tosylate.

20. The process of claim 1 , wherein the base in step (d) is selected from the group consisting of a metal carbonate, a metal hydroxide, a metal phosphate, and a metal hydride.

Assignees

• Dow Agrosciences Llc

Inventors

• Yang Qiang
• Lorsbach Beth
• Whiteker Greg
• Deamicis Carl
• Gray Kaitlyn
• Zhang Yu
• Muhuhi Joseck M

Classifications

• C07D231/38 Primary

  Nitrogen atoms (nitro radicals C07D231/16) · CPC title

• C07D401/14

  containing three or more hetero rings · CPC title

• C07D401/04 Primary

  directly linked by a ring-member-to-ring-member bond · CPC title

• A01N43/56 Primary

  1,2-Diazoles; Hydrogenated 1,2-diazoles · CPC title

• C07D231/40

  Acylated on said nitrogen atom · CPC title