Short and efficient synthesis of 5-aminothiazole-4-carboxamide
5-Aminothiazole-4-carboxamide is a precursor for the synthesis of thiazole [4,5-d] pyrimidines. In this work, a new synthesis method with a high total yield (79%) of 5-aminothiazole-4-carboxamide was reported. The starting material is aminocyanacetamide. This synthesis method is environment-friendly and is suitable for industrial production.
Wang, Jin,Guo, Jianyu,Tang, Yihong,Zhang, Suxia,Tao, Jianwei,Lu, Yan
p. 175 - 176
(2014/07/07)
Novel analogues of tiazofurin by Lawesson reagent effected cyclization
2-Benzylthiazole-4-carboxamide 4 and 5-(β-D-ribofuranosylamino) thiazole-4-carboxamide 10 were synthesized from phenylacetylamino- and formylamino cyanoacetic acid esters 1a and 1b, respectively. The ribosylation reaction leading to 10 gave rise also to i
Golankiewicz,Januszczyk
p. 313 - 316
(2007/10/02)
Azole series. I. Reaction of 2-(acylamino)thioacetamides, leading to 5-aminothiazoles and to thiazolo[5,4-d]pyrimidines.
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Sekiya,Osaki
p. 1319 - 1325
(2007/10/07)
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