IP Library Granted Patent US 7,329,633
Granted Patent B2
US 7,329,633 · App. 10/504,451 · Granted Feb 12, 2008

Disubstituted pyrazolylcarboxanilides

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Quick Facts
Patent No.
US 7,329,633
App. No.
10/504,451
Granted
Feb 12, 2008
Kind
B2
Abstract

This invention relates to novel pyrazolylcarboxanilides of formula (I) in which R, R 1 , R 2 and R 3 are as defined in the disclosure, to a plurality of processes for preparing these substances and their use for controlling unwanted microorganisms, and to novel intermediates and their preparation.

Claims (68)

1. A pyrazolylcarboxanilide of formula (I)

in which

R represents difluoromethyl or trifluoromethyl,

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, C 1 -C 6 -alkyl, C 2 -C 6 -alkenyl, C 1 -C 4 -alkoxy, C 1 -C 4 -alkylthio, C 1 -C 4 -alkylsulphonyl, or C 3 -C 6 -cycloalkyl; or represent C 1 -C 4 -haloalkyl, C 1 -C 4 -haloalkoxy, C 1 -C 4 -haloalkylthio, or C 1 -C 4 -haloalkylsulphonyl having in each case 1 to 5 halogen atoms, and

R 3 represents fluorine.

2. A pyrazolylcarboxanilide of formula (I) according to claim 1 in which

R represents difluoromethyl or trifluoromethyl,

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, methoxy, ethoxy, methylthio, ethylthio, n- or i-propylth io, cyclopropyl, trifluoromethyl, trichloromethyl, trifluoroethyl, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, difluoromethylthio, difluoroch loromethylthio, or trifluoromethylthio, and

R 3 represents fluorine.

3. A pyrazolylcarboxanilide of formula (I) according to claim 1 in which

R represents difluoromethyl or trifluoromethyl,

R 1 and R 2 independently of one another represent chlorine, bromine, methyl, trifluoromethyl, difluoromethoxy, or trifluoromethoxy, and

R 3 represents fluorine.

4. A pyrazolylcarboxanilide of formula (I) according to claim 1 in which R 1 represents methyl or trifluoromethyl.

5. A compound of formula (Ia)

in which

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, trifluoromethyl, trichloromethyl, trifluoroethyl, cyclopropyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, methylthio, ethylthio, n- or i-propylthio, difluoromethylthio, difluorochloromethylthio, or trifluoromethylthio, and

R 3 represents fluorine.

6. A compound of formula (Ib)

in which

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, trifluoromethyl, trichloromethyl, trifluoroethyl, cyclopropyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, methylthio, ethylthio, n- or i-propylthio, difluoromethylthio, difluorochloromethylthio, or trifluoromethylthio, and

R 3 represents fluorine.

7. A compound of formula (Ic)

in which

R represents difluoromethyl or trifluoromethyl,

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, trifluoromethyl, trichloromethyl, trifluoroethyl, cyclopropyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, methylthio, ethylthio, n- or i-propylthio, difluoromethylthio, difluorochloromethylthio, or trifluoromethylthio, and

R 3 represents fluorine.

8. A compound of formula (Id)

in which

R represents difluoromethyl or trifluoromethyl,

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, trifluoromethyl, trichloromethyl, trifluoroethyl, cyclopropyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, methylthio, ethylthio, n- or i-propylthio, difluoromethylthio, difluorochloromethylthio, or trifluoromethylthio, and

R 3 represents fluorine.

9. A compound of formula (Ie)

in which

R represents difluoromethyl or trifluoromethyl,

R 1 and R 2 independently of one another represent chlorine, bromine, cyano, nitro, methyl, ethyl, n- or i-propyl, n-, i-, s-, or t-butyl, trifluoromethyl, trichloromethyl, trifluoroethyl, cyclopropyl, methoxy, ethoxy, difluoromethoxy, trifluoromethoxy, difluorochloromethoxy, trifluoroethoxy, methylthio, ethylthio, n- or i-propylthio, difluoromethylthio, difluorochloromethylthio, or trifluoromethylthio, and

R 3 represents fluorine.

10. A process for preparing a pyrazolylcarboxanilide of formula (I) according to claim 1 comprising

(a) reacting a pyrazolylcarbonyl halide of formula (II)

in which

R is as defined for formula (I) in claim 1 , and

X 1 represents halogen,

 with an aniline derivative of formula (III)

in which R 1 , R 2 , and R 3 are as defined for formula (I) in claim 1 , optionally in the presence of an acid binder and optionally in the presence of a diluent, or

(b) reacting a halopyrazolecarboxanilide of formula (IV)

in which

R and R 3 are as defined for formula (I) in claim 1 , and

X 2 represents bromine or iodine,

 with a boronic acid derivative of formula (V)

in which

R 1 and R 2 are as defined for formula (I) in claim 1 , and

G 1 and G 2 each represent hydrogen or together represent tetramethylethylene,

 in the presence of a catalyst, optionally in the presence of an acid binder, and optionally in the presence of a diluent, or

(c) reacting In a first step a halopyrazolecarboxanillde of formula (IV)

in which

R and R 3 are defined for formula (I) in claim 1 , and

X 2 represents bromine or iodine,

 with a diborane derivative of formula (VI)

in which G 3 and G 4 each represent alkyl or together represent alkanedlyl,

 in the presence of a catalyst, optionally in the presence of an acid binder, and optionally in the presence of a diluent, and

 reacing without work-up in a second step with a haiobenzene derivative of the formula (VII)

in which

R 1 and R 2 are as defined for formula (I) in claim 1 , and

X 3 represents bromine, iodine, or trifluoromethylsulphonyloxy,

 in the presence of a catalyst, optionally in the presence of an acid binder, and optionally in the presence of a diluent.

11. A composition comprising one or more pyrazolylcarboxanilides of formula (I) according to claim 1 and one or more extenders and/or surfactants.

12. A method for controlling unwanted fungi comprising applying an effective amount of a pyrazolylcarboxanilide of formula (I) according to claim 1 to the fungi and/or their habitat.

13. A process for preparing a composition comprising mixing a pyrazolylcarboxanilide of formula (I) according to claim 1 with one or more extenders and/or surfactants.

Assignments (2)
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 11, 2019
From: BAYER INTELLECTUAL PROPERTY GMBH
To: BAYER CROPSCIENCE AKTIENGESELLSCHAFT
Reel/Frame 049359/0698 →
ASSIGNMENT OF ASSIGNOR'S INTEREST Recorded Jan 10, 2018
From: BAYER CROPSCIENCE AG
To: BAYER INTELLECTUAL PROPERTY GMBH
Reel/Frame 045034/0468 →