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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 2122023Erstellt: 26. Oktober 2026

Triethylamine → (2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic Acid

https://huagongshe.com/reaction/2122023

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktTriethylamineHCID 8471—
Edukt4'-Fluorobiphenyl-4-sulfonyl chlorideHCID 2794749—
Edukt(2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic acid methyl esterHCID 69881323—
Edukt(2S,3R)-2-amino-3-ethylsulfanyl-3-phenyl-propionic acid methyl esterHCID 69882615—
LösungsmittelDichloromethaneHCID 6344—
Produkt(2S,3R)-3-Ethylsulfanyl-2-(4'-fluoro-biphenyl-4-sulfonylamino)-3-phenyl-propionic AcidHCID 9825456—

Reaktionsschritte

(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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS06696456B1
Quelldatensatzuspto-grants-2004_02
ORD IDord-26b264d9ff03404fbef14fb6ef965191
Quellennotizuspto-grants-2004_02