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2-AMINO-4-METHYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE synthesis

1synthesis methods
7210-76-6 Synthesis
Ethyl 2-amino-4-methylthiazole-5-carboxylate

7210-76-6
243 suppliers
$5.00/1g

2-AMINO-4-METHYL-1,3-THIAZOLE-5-CARBOHYDRAZIDE

63788-59-0
8 suppliers
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Yield:-

Reaction Conditions:

with hydrazine hydrate in ethanol at 20; for 3 h;

Steps:

5.2. General procedure for preparation of 8a-d

General procedure: A mixture of substituted ethyl benzoate 2 (10 mmol) and hydrazinehydrate (20 mmol) in ethanol was stirred at room temperaturefor 3 h and then filtered. The crude product recrystallizedfrom absolute alcohol to give 3a-l, which were used directly forthe next step. Under this same condition, the intermediate compounds8a-d were also prepared.

References:

He, Haifeng;Wang, Wei;Zhou, Yuan;Xia, Qin;Ren, Yanliang;Feng, Jiangtao;Peng, Hao;He, Hongwu;Feng, Lingling [Bioorganic and Medicinal Chemistry,2016,vol. 24,# 8,p. 1879 - 1888]