Substituted phenoxymethylphenyl derivates, their preparation...

Details Substituted phenoxymethylphenyl derivates, their preparation... Substituted phenoxymethylphenyl derivates, their preparation...

C - Chemistry, Metallurgy

07

C

C07C 259/00 (2006.01) A01N 37/50 (2006.01) A01N 37/52 (2006.01) A01N 39/02 (2006.01) A01N 43/02 (2006.01) A01N 43/647 (2006.01) C07C 251/48 (2006.01) C07C 255/64 (2006.01) C07C 259/02 (2006.01) C07C 259/10 (2006.01) C07C 259/18 (2006.01) C07C 327/58 (2006.01) C07D 213/61 (2006.01) C07D 239/30 (2006.01) C07D 249/02 (2006.01) C07D 307/34 (2006.01) C07D 317/18 (2006.01) C07D 317/30 (2006.01) C07D 333/28 (2006.01) C07D 521/00 (2006.01)

Patent

CA 2145234

Substituted phenoxymethylphenyl derivatives I Image X is =CH-OCH3, =CH-CH3 or =N-OCH3; R1 is C1-C6-alkyl, C2-C6-alkenyl, C3-C6-alkynyl, C1-C6-haloalkyl, C3-C6-haloalkenyl, C1-C4-alkoxy-C1-C6--alkyl, cyano-C1-C6-alkyl, C1-C6-alkoxycarbonyl-C1-C6-alkyl, an unsubst. or subst. C3-C6-cycloalkyl or C3-C6-cycloalkyl-C1-C4-alkyl group, an unsubst. or subst. aryl-C1-C6-alkyl, aryl-C3-C6-alkenyl or aryloxy-C1-C6-alkyl group, an unsubst. or subst. heterocyclyl or heterocyclyl-C1-C4-alkyl or heteroaryl-C1-C6-alkyl group; R2 and R3 are H, halogen, CN, NO2, C1-C4-alkyl, C1-C2-haloalkyl, C1-C4-alkoxy, C1-C2-haloalkoxy,or, if R2 and R3 are adjacent, together are an unsubst. or subst. oxymethylidenoxy or oxyethylidenoxy bridge; R4 is CN, Cl, Br, C1-C6-alkoxy, C1-C6-alkylthio, C1-C4-haloalkoxy, C1-C4-alkoxy-C1-C4-alkoxy, C3-C6-cycloalkyl-C1-C2-alkoxy, C1-C6-alkylamino,di-(C1-C6-alkyl)amino, C3-C6-alkenyloxy, C3-C6-alkynyloxy, unsubst. or subst. aryloxy or arylthio; R5 is 2 NO2, CN, halogen, C1-C4-alkyl, C1-C4-haloalkyl, C1-C4-alkoxy, C1-C4-haloalkoxy, C1-C4-alkylthio, unsubst. or subst. phenyl or phenoxy, or, if n is 2, 3, or 4, an unsubst. or subst. 1,3-butadiene-1,4-diyl group fused to two adjacent C atoms of the parent substance; n is 0 - 4; Y is -O-, -NH-, -N(CH3)-; R6 is H, C1-C4-alkyl.

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