Reductive transformations of Schiff bases in the synthesis of functionally substituted heteroaromatic amines

…, AP Kadutskii, EV Koroleva, AV Baranovskii…

Index: Ignatovich; Kadutskii; Koroleva; Baranovskii; Gusak Russian Journal of Organic Chemistry, 2009 ,  vol. 45,  # 7  p. 1070 - 1078

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Citation Number: 6

Abstract

Abstract Schiff bases synthesized by condensation of 5-and 6-aminoquinolines, 5-amino-2- methylquinoline, nitroanilines, and pyrimidinylaminoanilines with substituted benzaldehydes and pyridinecarbaldehydes were reduced with sodium tetrahydridoborate in acetic acid to obtain the corresponding N-aryl (hetaryl) benzylamines, N-(pyridylmethyl) anilines, and N- (1, 2, 3, 4-tetrahydroquinolyl) benzylamine derivatives. The reduction of arylhetarylimines ...