Thiazole derivatives of 2-methoxyimino-2-(pyridinyloxymethyl)-phenyl-acetamides useful as fungicides

A compound according to formula one

• 7
• A is selected from the group consisting of oxy (—O—) and amino (—NH—);
• A1 is selected from the group consisting of oxo (O═) and thioxo (S═);
• E is selected from the group consisting of aza (—N═) and methine (—CH═);
• J1, J2, J3, and J4 are independently selected from the group consisting of hydro (—H), halo (—F, —Cl, —Br, and —I), C1-4 alkyl, C1-4 alkoxy, C1-4 alkyl (mono or multi- halo), and C1-4 alkylthio;
• M1, and M2 are selected from the group consisting of hydro (—H), halo (—F, —Cl, —Br, and —I), C1-6 alkyl, C1-6 alkoxy, C1-4 alkyl (mono or multi-halo), and C1-4 alkylthio, nitro (—NO2), (mono or multi-halo) C1-4 alkoxy, aryl (-Aryl), substituted aryl (—SAryl), heteroaryl (—HAryl), and substituted heteroaryl (—SHAryl), where “aryl” or “Ph” refers to a phenyl group and where “heteroaryl” refers to pyridyl, pyridinyl, pyrazinyl or pyridazinyl, and where said SAryl and SHAryl have substituents that are independently selected from the group consisting C1-C6 alkyl, C1-C6 alkoxy, halo-C1-C6 alkyl, halo-C1-C6 alkoxy, halo, nitro, carbo-C1-C6 alkoxy, or cyano, arylalkyl, alkanoyl, benzoyl, amino, and substituted amino, preferably, hydro (—H), C1-C6 alkyls, arylalkyl, alkanoyl, benzoyl, amino, and substituted amino where said substituted amino has substituents that are independently selected from the group consisting of hydro (—H), alkyl, arylalkyl, alkanoyl, benzoyl, and amino;
• Q is selected from the group consisting of hydro, halo, cyano, (mono or multi halo) C1-6 alkyl, and C1-6 alkyl;
• and
• T1 and T2 are independently selected from the group consisting of hydro (—H), halo (—F, —Cl, —Br, and —I), C1-6 alkyl, C1-6 alkoxy, C1-4 alkyl (mono or multi-halo), and C1-4 alkylthio, nitro (—NO2), (mono or multi-halo) C1-4 alkoxy, aryl (-Aryl), substituted aryl (—SAryl), heteroaryl (—HAryl), and substituted heteroaryl (—SHAryl), where “aryl” or “Ph” refers to a phenyl group and where “heteroaryl” refers to pyridyl, pyridinyl, pyrazinyl or pyridazinyl, and where said SAaryl and SHAryl have substituents that are independently selected from the group consisting C1-C6 alkyl, C1-C6 alkoxy, halo-C1-C6 alkyl, halo-C1-C6 alkoxy, halo, nitro, carbo-C1-C6 alkoxy, or cyano, arylalkyl, alkanoyl, benzoyl, amino, and substituted amino, preferably, hydro (—H), C1-C6 alkyls, arylalkyl, alkanoyl, benzoyl, amino, and substituted amino where said substituted amino has substituents that are independently selected from the group consisting of hydro (—H), alkyl, arylalkyl, alkanoyl, benzoyl, and amino. C1-4 alkyl or one of the single bonds can be the connecting bond to the pyridyl.