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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2426308생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/2426308

반응식

참여 물질

역할이름HCID투입량
반응물ChlorideHCID 312—
반응물1,2-DimethoxyethaneHCID 8071—
반응물Cesium fluorideHCID 25953—
반응물N-(5-Bromothiazol-2-yl)-N-methylacetamideHCID 67147803—
반응물methyl 2(S)-ethoxy-3-[4-(4,4,5,5-tetramethyl[1,3,2]dioxaborolan-2-yl)phenyl]propanoateHCID 67147872—
생성물methyl 3-{4-[2-(acetylmethylamino)thiazol-5-yl]phenyl}-2(S)-ethoxypropanoateHCID 8660623737%

반응 조건

온도80 °C

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07968560B2
출처 데이터셋uspto-grants-2011_06
ORD IDord-33f4ef09b01f40619de3308048ba19d6
출처 메모uspto-grants-2011_06