Chemical and Pharmaceutical Bulletin
Online ISSN : 1347-5223
Print ISSN : 0009-2363
ISSN-L : 0009-2363
Reaction of 6-Aminouracils with Ketenethioacetals
YOSHINORI TOMINAGASHINYA KOHRAHIROTO OKUDAATSUYUKI USHIROGOCHIYOSHIRO MATSUDAGORO KOBAYASHI
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1984 Volume 32 Issue 1 Pages 122-129

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Abstract
Reaction of ketenethioacetals [methyl 2-cyano-3, 3-bis (methylthio) acrylate (2), 3, 3-bis-(methylthio)-2-phenylsulfonylacrylonitrile (13)] with 6-aminouracils (1a : R1=R2=Me, 1b : R1=Ph, R2=H) in the presence of potassium carbonate followed by cyclization under reflux in diphenyl ether gave the corresponding 5-amino-6-methoxycarbonyl-7-methylthiopyrido [2, 3-d]-pyrimidine-2, 4 (1H, 3H)-dione derivatives (4a, b). Reaction of other ketenethioacetals [2-cyano-3, 3-bis (methylthio) acrylonitrile (10), dimethyl bis (methylthio) methylenemalonate (18), α-oxo ketenethioacetals (21a-e)] with 1 directly afforded pyrido [2, 3-d] pyrimidine derivatives (11a, b, 20a, b, 23a-e) in good yields. 5-Amino-7-methylthiopyrimido [4, 5-d] pyrimidine-2, 4 (1H, 3H)-dione derivatives (16a-c) were also synthesized from 6-aminouracils (1a, b) and dimethyl cyanoimidodithiocarbonate (15) in a manner similar to that used for the preparation of compound 11a.
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© The Pharmaceutical Society of Japan
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