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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

반응식

참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물4'-Fluorobiphenyl-4-sulfonyl chlorideHCID 2794749—
반응물(2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic acid methyl esterHCID 69881323—
반응물(2S,3R)-2-amino-3-ethylsulfanyl-3-phenyl-propionic acid methyl esterHCID 69882615—
용매DichloromethaneHCID 6344—
생성물(2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic AcidHCID 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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06696456B1
출처 데이터셋uspto-grants-2004_02
ORD IDord-26b264d9ff03404fbef14fb6ef965191
출처 메모uspto-grants-2004_02