A new scheme for the synthesis of pyrrolo2,3-dpyrimidines from monoacetylketene animals was proposed. Reactions of monoacetylketeneN-benzoyl- andN-acetylaminals with α-bromoacetophenone afforded the corresponding 3-acetyl-2-acylamino-5-phenyl- lH-pyr-roles, which underwent cyclization to 2,4,6-trisubstituted 7Hl-pyrrolo2,3-dpyrimidines under the action of ammonium acetate in boiling BuOH
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