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HRID 1919572作成日:2026年10月26日

Thioacetamide → Methyl 2-methyl-1,3-thiazole-5-carboxylate

https://huagongshe.com/reaction/1919572

反応式

関与物質

役割名称HCID仕込み量
反応物ThioacetamideHCID 2723949—
反応物Methyl 2-chloro-3-oxopropanoateHCID 14355182—
溶媒WaterHCID 962—
生成物Methyl 2-methyl-1,3-thiazole-5-carboxylateHCID 2142746543.6%

反応手順

2.0 g (14.6 mmol) methyl formylchloroacetate (A. Gangjee, A. Vidwans, E. Elzein, et. Al. J. Med. Chem. 2001, 44, 1993-2003), and 1.6 g (21.3 mmol) thioacetamide were dissolved in 10 ml water, heated, and reacted at 95° C. for 5 hr. The reaction product was extracted with ethyl acetate for 3 times, the ethyl acetate phases were combined, washed with a saturated sodium chloride solution, dried over anhydrous sodium sulfate, filtered, concentrated, and separated by a column chromatography to obtain 1.0 g methyl 2-methylthiazol-5-carboxylate (yield 43%), 1H NMR (CDCl3) 2.76 (3H, s), 3.89 (3H, s), 8.25 (1H, s).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08168642B2
出典データセットuspto-grants-2012_05
ORD IDord-aa214b6c6d174096a9f64c8cd4bbda1f
出典メモuspto-grants-2012_05