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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 732204생성일: 2026년 10월 26일

Phenacyl bromide → 3-{4-[(4-{[Benzyl(4-phenyl-1,3-thiazol-2-yl)amino]-methyl}benzyl)oxy]phenyl}propanoic acid

https://huagongshe.com/reaction/732204

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참여 물질

역할이름HCID투입량
반응물Phenacyl bromideHCID 6259—
반응물Sodium hydrideHCID 24758—
반응물N-(Phenylmethyl)thioureaHCID 737375—
반응물Methyl 3-(4-([4-(chloromethyl)benzyl]oxy)phenyl)propanoateHCID 23082857—
용매WaterHCID 962—
용매DimethylformamideHCID 6228—
생성물3-{4-[(4-{[Benzyl(4-phenyl-1,3-thiazol-2-yl)amino]-methyl}benzyl)oxy]phenyl}propanoic acidHCID 2314324241.2%

반응 조건

온도80 °C

반응 단계

A mixture of 2-bromo-1-phenylethanone (100 mg), N-benzylthiourea (83 mg) and N,N-dimethylformamide (2 mL) was stirred at 80° C. for 1 hr. The reaction mixture was cooled to 0° C., sodium hydride (60% in oil, 80 mg) was added, and the mixture was stirred at room temperature for 30 min. Methyl 3-(4-{[4-(chloromethyl)benzyl]oxy}phenyl)propanoate (300 mg) was added to the reaction mixture at room temperature, and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water and extracted with ethyl acetate. The ethyl acetate layer was dried using a Presep Dehydration tube (manufactured by Wako Pure Chemical Industries, Ltd.) and concentrated. The residue was purified by silica gel column chromatography (ethyl acetate:hexane=1:19-1:0 in volume ratio) to give the title compound (110 mg, yield 41%) as colorless crystals.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07585880B2
출처 데이터셋uspto-grants-2009_09
ORD IDord-a260857e28d7486193734f48abc86e6c
출처 메모uspto-grants-2009_09