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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2353372생성일: 2026년 10월 26일

Potassium Carbonate → 3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid tert-butyl ester

https://huagongshe.com/reaction/2353372

반응식

참여 물질

역할이름HCID투입량
반응물Potassium CarbonateHCID 11430—
반응물Tert-butyl 3-aminopropanoate hydrochlorideHCID 16218890—
반응물5-Bromomethyl-3-chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiopheneHCID 68452603—
용매DimethylformamideHCID 6228—
용매Ethyl AcetateHCID 8857—
생성물3-{[3-Chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid tert-butyl esterHCID 6845122876%

반응 조건

온도50 °C

반응 단계

To a solution of 5-bromomethyl-3-chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophene (50 mg, 0.104 mmol) in DMF (1 mL) are added β-alanine tert-butyl ester hydrochloride (19 mg, 1 eq.) and K2CO3 (68 mg, 5 eq.). The mixture is stirred at 50° C. overnight. The mixture is diluted with EtOAc (40 mL), washed with 10% aqueous Na2S2O3, brine, dried over MgSO4, filtered, and concentrated. The mixture is purified by column chromatography (EtOAc/Hexane, gradient) to give 43 mg of 3-{[3-chloro-2-(2-trifluoromethyl-biphenyl-4-yl)-benzo[b]thiophen-5-ylmethyl]-amino}-propionic acid tert-butyl ester in 76% yield.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07750021B2
출처 데이터셋uspto-grants-2010_07
ORD IDord-e6a1f26314a7438da9d6c59b2b825bed
출처 메모uspto-grants-2010_07