Claims
- 1. A compound of formula I whereinn is 0, 1, 2, 3 or 4, or, when R1 is nitro or cyano, n is 1 or 2, and wherein R1 can be the same or different if n is greater than 1; X is O or S; Y is a five-membered heteroaromatic ring which has 1-3 nitrogens and 2-4 carbons or 1-2 nitrogens, 1 oxygen or 1 sulfur, and 2-3 carbons which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3; R1 is nitro; cyano; halogen; C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy; C1-C4-alkylthio; phenyl or phenoxy, the aromatic rings may carry one to five halogen atoms or one to three of the following radicals selected from the group consisting of halogen, C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy and C1-C4-alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two of the following radicals selected from the group consisting of halogen, nitro, cyano, C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy and C1-C4-alkylthio; R2 is unsubstituted or substituted C1-C4 alkyl, unsubstituted or substituted C3-C6 cycloalkyl, or unsubstituted or substituted phenyl, cyano, acetyl or unsubstituted or substituted aromatic heterocycles containing one to three nitrogen and/or an oxygen or sulfur atom.
- 2. The compound of formula I according to claim 1, whereinn is 0, 1, 2, 3, or 4, or when R1 is nitro or cyano, n is 1 or 2, and wherein R1 can be the same or different if n is greater than 1; X is O or S; Y is selected from the group consisting of 3-isoxazolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 2-oxazolyl, 2-thiazolyl, 4-thiazolyl, 1,2,4-oxadiazol-5-yl, 1,2,4-thiadiazol-5-yl, 1, 2, 4, triazol-3-yl; 1,3,4-oxadiazol-2-yl; which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3; R1 is nitro; cyano; halogen; C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy; C1-C4-alkylthio; phenyl or phenoxy, wherein the aromatic rings may carry one to five halogen atoms or one to three radicals selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two radicals selected from the group consisting of halogen, nitro, cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; R2 is unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted phenyl, cyano, acetyl or unsubstituted or substituted aromatic heterocycles containing one to three nitrogen and/or an oxygen or sulfur atom.
- 3. The compound as claimed in claim 2, wherein Y is 3-isoxazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 4. The compound as claimed in claim 2, wherein Y is 1-pyrazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 5. The compound as claimed in claim 2, wherein Y is 3-pyrazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 6. The compound as claimed in claim 2, wherein Y is 4-pyrazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 7. The compound as claimed in claim 2, wherein Y is 2-oxazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 8. The compound as claimed in claim 2, wherein Y is 2-thiazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 9. The compound as claimed in claim 2, wherein Y is 4-thiazolyl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 10. The compound as claimed in claim 2, wherein Y is 1,2,4-oxadiazol-5-yl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 11. The compound as claimed in claim 2, wherein Y is 1,2,4-thiadiazol-5-yl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 12. The compound as claimed in claim 2, wherein Y is 1,2,4-oxadiazol-2-yl, which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3.
- 13. A composition for controlling harmful fungi, comprising a fungicidal amount of a compound of formula I according to claim 1 and an inert carrier.
- 14. A composition for controlling harmful insects, arachnids and nematodes comprising an effective amount of a compound of formula I according to claim 1 and an inert carrier.
- 15. A compound of formula I: wherein n is 0, 1, 2, 3 or 4, or, when R1 is nitro or cyano, n is 1 or 2, and wherein R1 can be the same or different if n is greater than 1,R1 is nitro, cyano, halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, phenyl or phenoxy which may have 1 to 5 halogen atoms or 1 to 3 of the following radicals: halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy and C1-C4 alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two of the following radicals: halogen, nitro, cyano, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy and C1-C4 alkylthio; R2 is unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted phenyl, cyano, acetyl or unsubstituted or substituted aromatic heterocycles containing one to three nitrogen and/or an oxygen or sulfur atom.
- 16. The compound according to claim 15, wherein R2 is phenyl which may be substituted with one or more radicals selected from the group consisting of halogen, cyano, C1-C4 alkyl, C1-C4 alkoxy, C1-C2 haloalkyl, C1-C2 haloalkoxy, phenyl and C1-C2-alkyldeneoxy.
- 17. A compound of the formula I, as claimed in claim 1, whereinn is 0, 1, 2, 3, or 4, or, when R1 is nitro or cyano, n is 1 or 2, and wherein R1 can be the same or different if n is greater than 1; X is O or S; Y is 1,2,4-triazol-3-yl, which may be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3; R1 is nitro; cyano; halogen; C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy; C1-C4-alkylthio; phenyl or phenoxy, wherein the aromatic rings can carry one to five halogen atoms or one to three radicals selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two radicals selected from the group consisting of halogen, nitro, cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; R2 is unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted phenyl, cyano, acetyl or unsubstituted or substituted aromatic heterocycles containing one to three nitrogen and/or an oxygen or sulfur atom.
- 18. A process for controlling harmful fungi, which comprises treating the harmful fungi, their environment or the plants or materials to be kept free of harmful fungi with a fungicidally effective amount of a compound of formula I whereinn is 0, 1, 2, 3, or 4, or, when R1 is nitro or cyano, n is 1 or 2, and wherein R1 can be the same or different if n is greater than 1; X is O or S; Y is a five-membered heteroaromatic ring which has 1-3 nitrogens and 2-4 carbons or 1-2 nitrogens, 1 oxygen or 1 sulfur, and 2-3 carbons which can be substituted with one or two radicals selected from the group consisting of Cl, CH3, CF3 and OCH3; R1 is nitro; cyano; halogen; C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy; C1-C4-alkylthio; phenyl or phenoxy, the aromatic rings may carry one to five halogen atoms or one to three radicals selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two radicals selected from the group consisting of halogen, nitro, cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; R2 is unsubstituted or substituted alkyl, unsubstituted or substituted cycloalkyl, unsubstituted or substituted phenyl, cyano, acetyl or unsubstituted or substituted aromatic heterocycles containing one to three nitrogen and/or an oxygen or sulfur atom.
- 19. A compound of formula I: wherein n is 0 or 1, and wherein R1 is nitro, cyano, halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy, C1-C4 alkylthio, phenyl or phenoxy which may have 1 to 5 halogen atoms or 1 to 3 of the following radicals: halogen, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy and C1-C4 alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two of the following radicals: halogen, nitro, cyano, C1-C4 alkyl, C1-C4 haloalkyl, C1-C4 alkoxy, C1-C4 haloalkoxy and C1-C4 alkylthio; R2 is 4-Cl—C6H4.
- 20. A compound of formula I whereinn is 0, 1, 2, 3, or 4, or, when R1 is nitro or cyano, n is 1 or 2, and wherein R1 can be the same or different if n is greater than 1; X is O or S; Y is a 1,2,4-triazole; R1 is nitro; cyano; halogen; C1-C4-alkyl; C1-C4-haloalkyl; C1-C4-alkoxy; C1-C4-haloalkoxy; C1-C4-alkylthio; phenyl or phenoxy, the aromatic rings may carry one to five halogen atoms or one to three radicals selected from the group consisting of halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; or, if n is greater than 1, a 1,3-butadiene-1,4-diyl group which is bonded to two adjacent C atoms of the phenyl radical and which may carry one to four halogen atoms or one or two radicals selected from the group consisting of halogen, nitro, cyano, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy and C1-C4-alkylthio; R2 is unsubstituted or substituted phenyl.
- 21. A compound of the formula
- 22. The compound of formula I according to claim 1, wherein Y is selected from the group consisting of 1-pyrrolyl, 2-pyrrolyl, 3-pyrrolyl, 3-isoxazolyl, 4-isoxazolyl, 5-isoxazolyl, 3-isothiazolyl, 4-isothiazolyl, 5-isothiazolyl, 1-pyrazolyl, 3-pyrazolyl, 4-pyrazolyl, 5-pyrazolyl, 2-oxazolyl, 4-oxazolyl, 5-oxazolyl, 2-thiazolyl, 4-thiazolyl, 5-thiazolyl, 1-imidazolyl, 2-imidazolyl, 4-imidazolyl, 1,2,4-oxadiazol-3-yl, 1,2,4-oxadiazol-5-yl, 1,2,4-thiadiazol-3-yl, 1,2,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl, 1,2,4-triazol-5-yl, 1,3,4-oxadiazol-2-yl, 1,3,4-thiadiazol-2-yl, 1,2,3-oxadiazol-4-yl, 1,2,3-oxadiazol-5-yl, 1,2,3-triazol-5-yl and 1,2,3-triazol-4-yl.
- 23. The compound of formula I according to claim 1, wherein Y is selected from the group consisting of 3-isoxazolyl, 3-pyrazolyl, 4-pyrazolyl-2-oxazolyl, 2-thiazolyl, 1,2,4-thiadiazol-5-yl, 1,2,4-triazol-3-yl.
Priority Claims (1)
Number |
Date |
Country |
Kind |
43 05 502 |
Feb 1993 |
DE |
|
Parent Case Info
This application is a Division of application Ser. No. 08/505,288 Filed on Aug. 21, 1995, now allowed which was originally filed as International Application Number PCT/EP94/00408 on Feb. 12, 1994 now U.S. Pat. No. 6,031,110.
US Referenced Citations (4)
Number |
Name |
Date |
Kind |
5395854 |
Brand et al. |
Mar 1995 |
A |
5856560 |
Bayer et al. |
Jan 1999 |
A |
5905087 |
Muller et al. |
May 1999 |
A |
6031110 |
Kirstgen et al. |
Feb 2000 |
A |