Potential Antimetabolites. III. Synthesis of 5-Aminoimidazole-4-carboxthioamide and Nitro-1-β-D-ribofuranosylimidazoles
5-Aminoimidazole-4-carboxthioamide was synthesized by the phosphorus pentasulfide-pyridine treatment of 5-aminoimidazole-4-carboxamide. The structure was elucidated both by chemical and physical means. 1-β-D-Ribofuranosy1-4-methyl-5-nitroimidazole and 1-β-D-ribofuranosy1-4-nitro-5-methoxycarbonylimi...
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Published in | Chemical & pharmaceutical bulletin Vol. 10; no. 8; pp. 660 - 664 |
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Main Authors | , , |
Format | Journal Article |
Language | English |
Published |
Japan
The Pharmaceutical Society of Japan
01.08.1962
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Subjects | |
Online Access | Get full text |
ISSN | 0009-2363 1347-5223 |
DOI | 10.1248/cpb.10.660 |
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Summary: | 5-Aminoimidazole-4-carboxthioamide was synthesized by the phosphorus pentasulfide-pyridine treatment of 5-aminoimidazole-4-carboxamide. The structure was elucidated both by chemical and physical means. 1-β-D-Ribofuranosy1-4-methyl-5-nitroimidazole and 1-β-D-ribofuranosy1-4-nitro-5-methoxycarbonylimidazole were synthesized by the condensation of appropriate imidazole chloro-mercury salt with 2, 3, 5-tri-Obenzoyl-D-ribofuranosyl chloride followed by the removal of protecting groups. |
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Bibliography: | ObjectType-Article-1 SourceType-Scholarly Journals-1 ObjectType-Feature-2 content type line 23 |
ISSN: | 0009-2363 1347-5223 |
DOI: | 10.1248/cpb.10.660 |