PROCESS FOR PREPARING PHENYLIMINO METHYL PYRIDINE DERIVATIVES

PROCESS FOR PREPARING PHENYLIMINO METHYL PYRIDINE DERIVATIVES

The title compds. I (X=H, cyano, alkoxy, cyclozlkyloxy, alkylthio, arylthio, alkyl, -NRR'; R=H, alkyl; R'=alkyl, aryl, cycloalkyl, acyl; Y, Z independently=halo, alkyl, alkoxy, nitro; m, n=0-2) were prepd. Thus, nicotine-4'-chloroanilide was treated with SOCl2 to give the imino chlori...

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Bibliographische Detailangaben
Hauptverfasser: HAKEN PIETER TEN, WEBB SHIRLEY BEATRICE, SMITH GRAHAM CLIFFORD
Format: Patent
Sprache:eng
Schlagworte:
CHEMISTRY
HETEROCYCLIC COMPOUNDS
METALLURGY
ORGANIC CHEMISTRY
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Zusammenfassung:The title compds. I (X=H, cyano, alkoxy, cyclozlkyloxy, alkylthio, arylthio, alkyl, -NRR'; R=H, alkyl; R'=alkyl, aryl, cycloalkyl, acyl; Y, Z independently=halo, alkyl, alkoxy, nitro; m, n=0-2) were prepd. Thus, nicotine-4'-chloroanilide was treated with SOCl2 to give the imino chloride, which was treated with CuCN to give 60% 4'-chlorophenylimino-C-(cyano)methyl-3-pyridine. At 1kg of the latter compd./ha there was >80% inhibition of plasmopera viticola on vine plants. Other compds. also had plant growth retardant and leaf abscission activity.