Synthesis and physiological activity of thiophenes and furans with 3- and 4-methoxyacetophenone derivatives

  • J Oleo Sci. 2008;57(2):107-13. doi: 10.5650/jos.57.107.
Shinya Tachibana  1 Takashi Gotou Masato Nomura
Affiliations
  • 1. Konan Chemical Industry Co., Ltd., Nakagawa, Takatsuki, Osaka 569-0066, Japan. [email protected]
Abstract

The synthesis and physiological activity of thiophenes and furans with methoxyacetophenone derivatives were examined. 3-Methoxyacetophenone (1) and 4-methoxyacetophenone (2) were converted, respectively, to the oximes (3) and (4) by oximation with hydroxylamine hydrochloride, and to the primary amines (5) and (6) by reduction with LiAlH(4). The primary amine derivatives were further converted into the thiophene and furan compounds (5a) approximately (5h) and (6a) approximately (6h), respectively. Bioassay of these compounds (5a) approximately (5h) and (6a) approximately (6h) on the germination of lettuce(Lactuca satiba) seeds showed that compound (5b) exhibits growthpromoting activity.

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