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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642287생성일: 2026년 10월 26일

Sodium hydride → 4-[(tert-Butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642287

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참여 물질

역할이름HCID투입량
반응물Sodium hydrideHCID 24758—
반응물Ethyl 2-((tert-butoxycarbonyl)amino)acetateHCID 357729—
반응물4-Bromomethyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic Acid Ethyl EsterHCID 17951768—
용매DimethylformamideHCID 6228—
생성물4-[(tert-Butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl esterHCID 6842740323.2%

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온도0 °C

반응 단계

A mixture of 4-bromomethyl-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester (1.05 g, 2.67 mmol), tert-butoxycarbonylamino-acetic acid ethyl ester (540 mg, 2.66 mmol) and sodium hydride (60% in mineral oil, 128 mg, 3.2 mmol) in anhydrous dimethylformamide (10 mL) was stirred at 0° C. for two hours and room temperature for half an hour before it was quenched with brine. The mixture was filtered and the filtrate was extracted with ethyl acetate. The organic layer was washed with water, brine, dried over anhydrous sodium sulfate and concentrated in vacuo. The residue was purified by flash column chromatography on silica gel with a gradient of ethyl acetate and hexanes to give the title compound as a yellow oil (319 mg): MS: (+) m/z 538.9 (M+Na+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696223B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-21d69a1fcdb84e4cb15db075e3f583f3
출처 메모uspto-grants-2010_04