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Several new pyrimidines 6–11, 18–20, furo‐, thieno‐, and pyrrolo[2,3‐d]pyrimidines 3, 8, 12, triazolo‐[4,3‐a]pyrimidines 14, 15, 16 and tetrazolo[1,5‐a]pyrimidine 17 were prepared from the known intermediate 5‐(2‐hydroxyethyl)‐6‐methyl‐2‐thiouracil (2). Compound 7 (4‐chloro‐5‐(2‐chloroethyl)‐2‐methylthio‐6‐methyl‐pyrimidine) exhibited weak antitumor activity in vitro.
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E.‐S. A. M. BADAWEY (1996) studied this question.
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