Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2122023생성일: 2026년 10월 27일
Triethylamine → (2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic Acid
https://huagongshe.com/reaction/2122023
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethylamine | HCID 8471 | — |
| 반응물 | 4'-Fluorobiphenyl-4-sulfonyl chloride | HCID 2794749 | — |
| 반응물 | (2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic acid methyl ester | HCID 69881323 | — |
| 반응물 | (2S,3R)-2-amino-3-ethylsulfanyl-3-phenyl-propionic acid methyl ester | HCID 69882615 | — |
| 용매 | Dichloromethane | HCID 6344 | — |
| 생성물 | (2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic Acid | HCID 9825456 | — |
반응 단계
(2S,3R)-3-Ethylsulfanyl-2-(4′-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic acid methyl ester. To a solution of (2S,3R)-2-amino-3-ethylsulfanyl-3-phenyl-propionic acid methyl ester 4a (49 mg, 0.20 mmol) in methylene chloride (2.0 mL) is added triethylamine (0.060 mL, 0.43 mmol) and 4′-fluoro-4-biphenylsulfonyl chloride (66 mg, 0.24 mmol). This mixture is stirred under argon overnight at room temperature. The reaction is diluted with methylene chloride and washed with 1.0 N aq. HCl. The aqueous layer is extracted with methylene chloride. The combined organic layers are dried over Na2SO4, filtered, and concentrated under reduced pressure. The crude product is purified by column chromatography (silica gel, 20% EtOAc/hexanes) to give the desired product.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US06696456B1 |
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| 출처 데이터셋 | uspto-grants-2004_02 |
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| ORD ID | ord-26b264d9ff03404fbef14fb6ef965191 |
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| 출처 메모 | uspto-grants-2004_02 |
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