FIELD: organic synthesis. SUBSTANCE: invention provides novel phenylacetic acid derivatives of general formula I: (I), in which X denotes NOCH3, CHOCH3 and CHCH2CH3; R1 hydrogen or C1-C4-alkyl; R2 halogen, C1-C4-alkyl, or C1- C4-alkoxy; m= 0 or 1; R3 denotes hydrogen, amino, halogen, C1-C4-alkyl, C1- C4-haloalkyl, C1-C4-alkoxy, C1-C4-alkylthio, C1-C4-alkylamino, or di- C1- C4-alkylamino; R4 cyano, halogen, C1-C6-alkyl, C1-C6-alkoxy, C2-C6- alkenyl, C2-C6-alkenyloxy, or C2-C6-alkinyl; provided that hydrocarbon moieties of above-indicated groups can be partially or completely halogenated or can bear one to three substituents selected from cyano, C1- C6-alkoxy, C1-C6-alkoxycarbonyl, phenyl, and dioxan (cyclic radicals can be partially or completely halogenated), C3-C6-cycloalkyl, C3-C6-cycloalkenyl, aryl, isoxazolyl, pyridyl, dioxolanyl, benzoxazolyl, thienyl, oxazolyl, furyl, oxyranyl, pyrazolyl, thiazolyl, pyrimidyloxy or tetrahydropyranyl, provided that cyclic radicals can be partially or completely halogenated or can bear one to three substituents selected from nitro, C1-C6-alkyl, C1-C6- alkoxy, C1-C6-haloalkyl, C1-C6-alkylamino, di-C1-C6-alkylamino and aryl; R5 denotes hydrogen, C1-C10-alkyl, C2-C10-alkenyl, or C2-C10-alkinyl, provided that these radicals can be partially or completely halogenated or can bear one to three substituents selected from cyano, hydroxy, aminocarbonyl, C1-C6-alkyl, C2-C6-alkenyl, C1-C6-alkoxycarbonyl, C1-C6- alkylamino, benzyl, aryl, aryloxy, thienyl, pyrrolyl, oxazolyl, furyl, thiazolyl, oxadiazolyl, and isoxazolyl, cyclic radicals themselves can be partially or completely halogenated or can bear one to three substituents selected from nitro, hydroxy, C1-C4-alkyl, C1-C4-haloakyl, and C3-C6- cycloalkyl; on condition that X cannot be NOCH3 and CHOCH3, when R4 is unsubstituted C1-C4-alkyl, unsubstituted C3-C6-cycloalkyl, substituted or unsubstituted phenyl, or unsubstituted thienyl; or X cannot be CHOCH3, when R3 is hydrogen and R5 is C1-C10-alkyl; as well as salts or above-indicated compounds. Compound I show fungicidal activity. EFFECT: extended choice of active fungicides. 8 cl, 16 tbl, 10 ex
Title | Year | Author | Number |
---|---|---|---|
DERIVATIVES OF PHENYLACETIC ACID AND AGENT FOR CONTROL AGAINST INSECTS AND SPIDER-LIKE AND DELETERIOUS FUNGI | 1995 |
|
RU2162075C2 |
2-[1',2',4'-TRIAZOLE-3'-YLOXYMETHYLENE]-ANILIDES, INTERMEDIATE COMPOUNDS AND AGENT FOR CONTROL OF HARMFUL FUNGI | 1995 |
|
RU2165927C2 |
2-[(DIHYDRO)PYRAZOLYL-3-OXYMETHYLENE]ANILIDES METHOD OF PREPARATION THEREOF, INTERMEDIATE COMPOUNDS, AGENT FOR CONTROLLING AGRICULTURAL PESTS AND HARMFUL FUNGI, AND CONTROL METHODS | 1995 |
|
RU2151142C1 |
2-IMINOOXYPHENYL ACETIC ACID DERIVATIVES, AND AGENT COMPRISING SAID COMPOUNDS | 1996 |
|
RU2170229C2 |
IMINOOXIMETHYLENEANILIDES, METHOD OF PREPARATION THEREOF (VERSIONS), PEST-CONTROL AGENTS, PEST-CONTROL METHOD, AND INTERMEDIATE COMPOUNDS | 1995 |
|
RU2143423C1 |
METHODS AND INTERMEDIATE PRODUCTS FOR PREPARING ALPHA- METHOXYIMINOCARBOXYLIC ACID METHYLAMIDES | 1995 |
|
RU2146247C1 |
HARMFUL FUNGI CONTROL AGENT AND METHOD | 1996 |
|
RU2158083C1 |
METHOD FOR PREPARING OPTICALLY ACTIVE AMINES (VARIANTS) AND OPTICALLY ACTIVE AMINE | 2000 |
|
RU2293724C9 |
SUBSTITUTED DERIVATIVES OF PYRAZINE AND HERBICIDE AGENT BASED ON THEREOF | 1995 |
|
RU2155756C2 |
METHOD OF SYNTHESIS OF OXIME ESTERS BY INTERACTION OF OXAMINE WITH DIALKYLCARBONATES | 1995 |
|
RU2167149C2 |
Authors
Dates
2001-04-20—Published
1995-01-03—Filed