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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 642288생성일: 2026년 10월 27일

Potassium tert-butoxide → 7-Hydroxy-2-(4-trifluoromethyl-phenyl)-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl ester

https://huagongshe.com/reaction/642288

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참여 물질

역할이름HCID투입량
반응물Potassium tert-butoxideHCID 23665647—
반응물4-[(tert-Butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl esterHCID 68427403—
용매TetrahydrofuranHCID 8028—
생성물7-Hydroxy-2-(4-trifluoromethyl-phenyl)-thiazolo[4,5-c]pyridine-6-carboxylic acid ethyl esterHCID 684264220.1%

반응 조건

온도-78 °C

반응 단계

A mixture of 4-[(tert-butoxycarbonyl-ethoxycarbonylmethyl-amino)-methyl]-2-(4-trifluoromethyl-phenyl)-thiazole-5-carboxylic acid ethyl ester (302 mg, 0.58 mol) in THF (5 mL) was added drop wise a solution of 1 M KOtBu in THF (702 μL, 0.70 mmol) at −78° C. The mixture was stirred at −78° C. for 15 min, warmed to room temperature and stirred at that temperature for 1.5 h before it was quenched with brine, extracted with ethyl acetate. The organic layer was washed with brine, dried over anhydrous sodium sulfate and concentrated in vacuo to a yellow foam (469 mg). It was dissolved in dichloromethane (10 mL) and TFA (2.5 mL) was added. The mixture was stirred at room temperature for 1 h before it was concentrated in vacuo. It was redissolved in dichloromethane, triethylamine (923 μL) was added. The mixture was stirred under air overnight before it was partitioned between dichloromethane and water, the organic layer was washed with 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 dichloromethane to give the title compound as a white solid (257 mg): MS: (+) m/z 330.0 (M+1).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07696223B2
출처 데이터셋uspto-grants-2010_04
ORD IDord-b15059aad254442bb9d0e7ba1480cbf3
출처 메모uspto-grants-2010_04