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1. (WO1991007400) PYRIMIDINE DERIVATIVES, PROCESS FOR MAKING THEM, AGENTS CONTAINING THEM AND THEIR USE AS FUNGICIDES
Latest bibliographic data on file with the International Bureau

Pub. No.: WO/1991/007400 International Application No.: PCT/EP1990/001858
Publication Date: 30.05.1991 International Filing Date: 07.11.1990
Chapter 2 Demand Filed: 29.05.1991
IPC:
A01N 43/54 (2006.01) ,C07D 401/04 (2006.01)
A HUMAN NECESSITIES
01
AGRICULTURE; FORESTRY; ANIMAL HUSBANDRY; HUNTING; TRAPPING; FISHING
N
PRESERVATION OF BODIES OF HUMANS OR ANIMALS OR PLANTS OR PARTS THEREOF; BIOCIDES, e.g. AS DISINFECTANTS, AS PESTICIDES OR AS HERBICIDES; PEST REPELLANTS OR ATTRACTANTS; PLANT GROWTH REGULATORS
43
Biocides, pest repellants or attractants, or plant growth regulators containing heterocyclic compounds
48
having rings with two nitrogen atoms as the only ring hetero atoms
54
1,3-Diazines; Hydrogenated 1,3-diazines
C CHEMISTRY; METALLURGY
07
ORGANIC CHEMISTRY
D
HETEROCYCLIC COMPOUNDS
401
Heterocyclic compounds containing two or more hetero rings, having nitrogen atoms as the only ring hetero atoms, at least one ring being a six-membered ring with only one nitrogen atom
02
containing two hetero rings
04
directly linked by a ring-member-to-ring- member bond
Applicants:
HOECHST AKTIENGESELLSCHAFT [DE/DE]; Postfach 80 03 20 D-6230 Frankfurt am Main 80, DE (AllExceptUS)
GIENCKE, Wolfgang [DE/DE]; DE (UsOnly)
SACHSE, Burkhard [DE/DE]; DE (UsOnly)
WICKE, Heinrich [DE/DE]; DE (UsOnly)
Inventors:
GIENCKE, Wolfgang; DE
SACHSE, Burkhard; DE
WICKE, Heinrich; DE
Common
Representative:
HOECHST AKTIENGESELLSCHAFT; Zentrale Patentabteilung Postfach 80 03 20 D-6230 Frankfurt am Main 80, DE
Priority Data:
P 39 37 284.709.11.1989DE
Title (DE) PYRIMIDIN-DERIVATE, VERFAHREN ZU IHRER HERSTELLUNG, SIE ENTHALTENDE MITTEL UND IHRE VERWENDUNG ALS FUNGIZIDE
(EN) PYRIMIDINE DERIVATIVES, PROCESS FOR MAKING THEM, AGENTS CONTAINING THEM AND THEIR USE AS FUNGICIDES
(FR) DERIVES DE LA PYRIMIDINE, LEUR PROCEDE DE FABRICATION, PRODUITS LES RENFERMAMT ET LEUR UTILISATION COMME FONGICIDES
Abstract:
(DE) Verbindungen der Formel (I), worin R1 = Wasserstoff, Alkyl, Alkoxyalkyl, Alkylthioalkyl, Alkenyl, Alkinyl, Cycloalkyl, Cycloalkylalkyl, wobei die beiden letztgenannten Reste im Cycloalkylteil substituiert sein können, Phenyl, Phenoxyalkyl, Phenylmercaptoalkyl, Phenylalkyl, Phenoxy-phenoxyalkyl, wobei diese Rest im Phenylteil substituiert sein können, R2, R3, R4 = unabhängig voneinander Wasserstoff, Alkyl, (subst.) Phenyl, R5 = Wasserstoff, Alkyl, Cycloalkyl, Cycloalkylalkyl, wobei diese beiden Reste im Cycloalkylteil substituiert sein können, Haloalkyl, Alkoxy, Alkylthio, Alkoxyalkyl, Alkylthioalkyl, Halogen, Alkenyl, Alkinyl, Phenyl, Phenoxy, Phenylalkyl, Phenoxyalkyl, Phenylmercaptoalkyl, Phenylmercapto, Phenylalkoxy oder Phenylalkylthio, wobei diese Reste im Phenylteil substituiert sein können, Alkenyloxy, Alkinyloxy, Haloalkoxy, Alkoxyalkoxy, Alkylthioalkylthio, R6 = Wasserstoff, Alkyl, Alkoxy, Alkenyloxy, Alkinyloxy, Alkylthio, Halogen, Phenyl, wobei der Phenylrest substituiert sein kann. R7, R8, R9, R10 = unabhängig voneinander Wasserstoff, Halogen, Nitro, Cyano, Alkyl, Alkoxy, Alkylthio, Haloalkyl oder Haloalkoxy, R11, R12 = unabhängig voneinander Wasserstoff oder Alkyl und n = 1 - 3, sowie deren Säureadditionssalze besitzen vorteilhafte fungizide Eigenschaften.
(EN) Compounds of formula (I) in which: R1 = hydrogen, alkyl, alkoxyalkyl, alkylthioalkyl, alkenyl, alkinyl, cycloalkyl, cycloalkylalkyl, whereby the two last-mentioned residues may be substituted in the cycloalkyl part, phenyl, phenoxyalkyl, phenylmercaptoalkyl, phenylalkyl, phenoxy-phenoxyalkyl, whereby these residues may be substituted in the phenyl part; R2, R3, R4 = mutually independently hydrogen, alkyl, (subst.) phenyl; R5 = hydrogen, alkyl, cycloalkyl, cycloalkylalkyl, whereby these two residues may be substituted in the cycloalkyl part, haloalkyl, alkoxy, alkylthio, alkoxyalkyl, alkylthioalkyl, halogen, alkenyl, alkinyl, phenyl, phenoxy, phenylalkyl, phenoxyalkyl, phenylmercaptoalkyl, phenylmercapto, phenylalkoxy or phenylalkylthio, whereby these residues may be substituted in the phenyl part, alkenyloxy, alkinyloxy, haloalkoxy, alkoxyalkoxy, alkylthioalkylthio; R6 = hydrogen, alkyl, alkoxy, alkenyloxy, alkinyloxy, alkylthio, halogen, phenyl, whereby the phenyl residue may be substituted; R7, R8, R9, R10 = mutually independently hydrogen, halogen, nitro, cyano, alkyl, alkoxy, alkylthio, haloalkyl or haloalkoxy; R11, R12 = mutually independently hydrogen or alkyl; and n = 1 - 3, and their acid addition salts have advantageous fungicidal properties.
(FR) Des procédés ayant la formule (I) dans laquelle R1 représente un hydrogène, alkyle, alkoxyalkyle, alkylthioalkyle, alkényle, alkinyle, cycloalkyle, cycloalkylalkyle, les deux derniers résidus précités pouvant être substitués dans la partie cycloalkyle, ainsi que les résidus phényle, phénoxyalkyle, phénylmercaptoalkyle, phénylalkyle, phénoxy-phénoxyalkyle, ces résidus pouvant être substitués dans la partie phényle, R2, R3, R4, représentent, indépendamment les uns des autres, un hydrogène, alkyle, phényle (substitué), R5 est un hydrogène, alkyle, cycloalkyle, cycloalkylalkyle, ces deux résidus pouvant être substitués dans la partie cycloalkyle, ainsi que les résidus halo-alkyle, alkoxy, alkylthio, alkoxyalkyle, alkylthioalkyle, halogène, alkényle, alkinyle, phényle, phénoxy, phénylalkyle, phénoxyalkyle, phénylmercaptoalkyle, phénylmercapto, phénylalkoxy ou phénylalkylthio, ces résidus pouvant être substitués dans la partie phényle, ainsi que les résidus alkényloxy, alkinyloxy, haloalkoxy, alkoxyalkoxy, alkylthioalkylthio, R6 est un hydrogène, alkyle, alkoxy, alkényloxy, alkinyloxy, alkylthio, halogène, phényl, le résidu phényle pouvant être substitué, R7, R8, R9, R10 représentent, indépendamment les uns des autres, un hydrogène, nitro, cyano, alkyle, alkoxy, alkylthio, haloalkyle ou haloalkoxy, R11, R12 sont, indépendamment les uns des autres, un hydrogène ou un alkyle, et n = 1 - 3, ainsi que leurs sels d'addition d'acide, possèdent des propriétés fongicides avantageuses.
Designated States: AU, BR, CA, HU, JP, KR, SU, US
European Patent Office (AT, BE, CH, DE, DK, ES, FR, GB, GR, IT, LU, NL, SE)
Publication Language: German (DE)
Filing Language: German (DE)
Also published as:
EP0518862JPH05501550CA2068328PT95831KR1019927003569AU1990066389