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HRID 1864546作成日:2026年10月26日

Chloride → methyl 3-{4-[2-(acetylmethylamino)thiazol-5-yl]phenyl}-2(S)-ethoxypropanoate

https://huagongshe.com/reaction/1864546

反応式

関与物質

役割名称HCID仕込み量
反応物ChlorideHCID 312—
反応物1,2-DimethoxyethaneHCID 8071—
反応物Cesium fluorideHCID 25953—
反応物N-(5-Bromothiazol-2-yl)-N-methylacetamideHCID 67147803—
反応物methyl 2(S)-ethoxy-3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]propanoateHCID 67147872—
生成物methyl 3-{4-[2-(acetylmethylamino)thiazol-5-yl]phenyl}-2(S)-ethoxypropanoateHCID 8660623737%

反応条件

温度80 °C

反応手順

0.2 g (0.3 mmol) of diphenylphosphinoferrocenepalladium chloride (PdCl2dppf) is added to a solution of 1 g (4.5 mmol) of N-(5-bromothiazol-2-yl)-N-methylacetamide, 1.8 g (6.8 mmol) of methyl 2(S)-ethoxy-3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]propanoate and 1 g (6.8 mmol) of caesium fluoride in 50 ml of ethylene glycol dimethyl ether, degassed beforehand. The reaction medium is heated at 80° C. for 18 hours. After cooling, water is added and the reaction medium is extracted with ethyl acetate. The ethyl acetate phase is washed with saturated sodium chloride solution, dried over magnesium sulfate, filtered and evaporated. The residue obtained is purified by chromatography on a column of silica eluted with a 70/30 and then 60/40 heptane/ethyl acetate mixture. 0.6 g (37%) of methyl 3-{4-[2-(acetylmethylamino)thiazol-5-yl]phenyl}-2(S)-ethoxypropanoate is obtained in the form of a beige-colored solid with a melting point of 123° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07625914B2
出典データセットuspto-grants-2009_12
ORD IDord-de25fe6d5d264d35b574712ee5f4b830
出典メモuspto-grants-2009_12