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2000
Volume 5, Issue 4
  • ISSN: 1570-1786
  • E-ISSN: 1875-6255

Abstract

An efficient one-step conversion of 4-phenyl-5-ethoxycarbonyl-3-cyano-6-metlyl-2(1H)-pyridone (1) into ethyl 3-amino-6-methyl-4-phenyl-1H-pyrazolo[3,4-b]pyridine-5-carboxylate (7) is described. An unusual hydrazine mediated decarboxylation of 7 into 3-amino-6-methyl-4-phenyl-1H-pyrazolo[3,4-b]pyridine (8) is reported. The structure of 8 was confirmed by spectral and chemical investigations. A plausible reaction mechanism for the formation of the unexpected product 8 is proposed.

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/content/journals/loc/10.2174/157017808784049416
2008-06-01
2025-09-09
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/content/journals/loc/10.2174/157017808784049416
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  • Article Type:
    Research Article
Keyword(s): cyanopyridone; decarboxylation; hydrazine; One-step conversion; pyrazolo[3,4-b]pyridine
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