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
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Phenacyl bromide | HCID 6259 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | N-(Phenylmethyl)thiourea | HCID 737375 | — |
| 반응물 | Methyl 3-(4-([4-(chloromethyl)benzyl]oxy)phenyl)propanoate | HCID 23082857 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 3-{4-[(4-{[Benzyl(4-phenyl-1,3-thiazol-2-yl)amino]-methyl}benzyl)oxy]phenyl}propanoic acid | HCID 23143242 | 41.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07585880B2 |
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| 출처 데이터셋 | uspto-grants-2009_09 |
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| ORD ID | ord-a260857e28d7486193734f48abc86e6c |
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| 출처 메모 | uspto-grants-2009_09 |
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