Dihydropyridazinones and pyridazinones their use as...

C - Chemistry – Metallurgy – 07 – D

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C07D 237/14 (2006.01) A01N 47/24 (2006.01) A01N 55/10 (2006.01) A01N 57/24 (2006.01) C07D 237/04 (2006.01) C07D 237/24 (2006.01) C07D 401/02 (2006.01) C07D 403/02 (2006.01) C07D 405/02 (2006.01) C07D 409/02 (2006.01) C07D 413/02 (2006.01) C07D 417/02 (2006.01) C07F 7/10 (2006.01) C07F 9/6509 (2006.01)

Patent

CA 2216512

Compounds with fungicidal and insecticidal properties having formula I Image (I) wherein W is Image n is 0 or 1; Y is O, S, NR1, or R6; the ring bond containing R4 and R5 is a single or double bond; X is independently selected from hydrogen, halo, (C1-C4)alkyl, (C1-C4)alkoxy and -HC=CH-CH=CH- thereby forming a napthyl ring; R is independently selected from (C1-C12)alkyl and halo(C1-C12)alkyl; R1 is independently selected from (C1-C12)alkyl, (C2-C8)alkenyl and aryl; R2 is independently selected from hydrogen, (C1-C12)alkyl, (C1-C12)alkoxy, halo(C1-C12)alkyl, halo(C1-C12)alkoxy, hydroxy(C1-C12)alkyl, (C1-C12)alkoxy(C1-C12)alkyl, (C1-C12)alkoxycarbonyl(C1-C12)alkyl, (C2-C8)alkenyl, halo(C2-C8)alkenyl, (C3-C10)alkynyl, halo(C3-C10)alkynyl, (C3-C7)cycloalkyl, (C3-C7)cycloalkyl(C1-C4)alkyl, epoxy(C1-C12)alkyl, PO(OR1)2(C1-C12)alkyl, R1S(O)2(C1-C12)alkyl, (R1)3Si(C1-C12)alkyl, aryl, aryloxy(C1-C12)alkyl, arylcarbonyl(C1-C12)alkyl, aralkyl, arylalkenyl, heterocyclic, heterocyclic (C1-C12)alkyl, N-morpholino(C1-C12)alkyl, N-piperidinyl(C1-C12)alkyl; R4, and R5 are independently selected from hydrogen, halo, (C1-C8)alkyl, (C1-C8)alkoxy, cyano, halo(C1-C12)alkyl, (C2-C8)alkenyl, (C3-C10 )alkynyl, aryl and aralkyl; and R6 is (C1-C12) alkylenyl and (C2-C12)alkenylenyl. 31

Composés dotés de propriétés fongicides et insecticides de formule I Image (I) où W est Image n est 0 ou 1; Y est O, S, NR1 ou R6; la liaison sur le noyau contenant R4 et R5 peut être simple ou double; X est, indépendamment, un atome d'hydrogène, un halo, un alkyle en C1-C4, un alcoxy en C1-C4 et -HC=CH-CH=CH- formant ainsi un noyau naphtyle; R est, indépendamment, un alkyle en C1-C12 et un haloalkyle en C1-C12; R1 est, indépendamment, un alkyle en C1-C12, un alkényle en C2-C8 et un aryle; R2 est, indépendamment, un atome d'hydrogène, un alkyle en C1-C12, un alcoxy en C1-C12, un haloalkyle en C1-C12, un haloalcoxy en C1-C12, un hydroxyalkyle en C1-C12, un alcoxy en C1-C12-alkyle en C1-C12, un alcoxy en C1-C12-carbonyle-alkyle en C1-C12, un alkényle en C2-C8, un haloalkényle en C2-C8, un alkynyle en C3-C10, un haloalkynyle en C3-C10, un cycloalkyle en C3-C7, un cycloalkyle en C3-C7-alkyle en C1-C4, un époxyalkyle en C1-C12, un PO(OR1)2-alkyle en C1-C12, un R1S(O)2-alkyle en C1-C12, un (R1)3Si-alkyle en C1-C12, un aryle, un aryloxyalkyle en C1-C12, un arylcarbonylalkyle en C1-C12, un aralkyle, un arylalkényle, un alkyle en C1-C12 hétérocyclique, un N-morpholinoalkyle en C1-C12, un N-pipéridinylalkyle en C1-C12; R4 et R5 sont, indépendamment, un atome d'hydrogène, un halo, un alkyle en C1-C8, un alcoxy en C1-C8, un cyano, un haloalkyle en C1-C12, un alkényle en C2-C8, un alkynyle en C3-C10, un aryle et un aralkyle; et R6 est un alkylényle en C1-C12 et un alkénylényle en C2-C12.

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