2-Alkyl-1-alkylthioisoquinolinium salts were readily prepared from 2-alkyl-1(2H)-isoquinolones via 2-alkyl-1(2H)-thioisoquinolones in two steps. Under mild conditions, the reaction of 2-alkyl-l-alkylthioisoquinolinium salts with active methylene compounds in the presence of sodium hydride afforded 2-alkyl-1-(substituted methylene) iso-quinolines in good yields. Pyrrolo[2,1-a]isoquinolines were synthesized by the cyclization of 2-benzyl-1-(substituted methylene)isoquinolines using acetic anhydride. © 2002 Pharmaceutical Society of Japan.
CITATION STYLE
Fujita, R., Watanabe, N., & Tomisawa, H. (2002). Reaction of 1-alkylthioisoquinolinium salts with active methylene compounds. Chemical and Pharmaceutical Bulletin, 50(2), 225–228. https://doi.org/10.1248/cpb.50.225
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