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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1884279Generated: November 2, 2026

Water → 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-hydroxy-5-(phenylthio)-pentanoic Acid

https://huagongshe.com/reaction/1884279

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactantm-Chloroperbenzoic acidHCID 70297—
ReactantMethyl 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4,5-epoxypentanoateHCID 23508251—
ReactantMethyl 2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-pentenoateHCID 23508264—
SolventDichloromethaneHCID 6344—
SolventSodium BicarbonateHCID 516892—
Product2-[[(1,1'-biphenyl)-4-yl]sulfonyl]amino-4-hydroxy-5-(phenylthio)-pentanoic AcidHCID 23508293—

Reaction Steps

Methyl 2-[[(1,1′-biphenyl)-4-yl]sulfonyl]amino-4,5-epoxypentanoate: To a solution of methyl 2-[[(1,1′-biphenyl)-4-yl]sulfonyl]amino-4-pentenoate 16a (2.0 g, 5.8 mmol) in CH2Cl2 (15 mL), NaHCO3 (0.58 g, 7 mmol) and water (10 mL) at 0° C., is added slowly m-chloroperbenzoic acid (3.3 g, 11.6 mmol, 57-86%). The reaction mixture is stirred overnight. The resulting mixture is diluted with aqueous NaHCO3, and the mixture is extracted three times with CH2Cl2. The combined CH2Cl2 layers are washed with NaHCO3, brine, dried over MgSO4 and concentrated to an oil which is purified by column chromatography eluting with EtOAc/hexane (4:6) to give the desired product as a mixture of two isomers (ratio 2:3).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06762198B2
Source datasetuspto-grants-2004_07
ORD IDord-89872ee1d6be4bb0bfbe4c48058c7d55
Source noteuspto-grants-2004_07