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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 874562Generated: October 30, 2026

Water → methyl (S)-3-(4-benzyloxybenzenesulfonylamino)-2-(4-methanesulfonylpiperazin-1-yl)propanoate

https://huagongshe.com/reaction/874562

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-(Benzyloxy)benzene-1-sulfonyl chlorideHCID 4738385—
ReactantMethyl (S)-3-amino-2-(4-methanesulfonylpiperazin-1-yl)propanoate dihydrochlorideHCID 86675013—
SolventDichloromethaneHCID 6344—
Productmethyl (S)-3-(4-benzyloxybenzenesulfonylamino)-2-(4-methanesulfonylpiperazin-1-yl)propanoateHCID 86675014—

Reaction Steps

1.1 ml (7.8 mmol) of triethylamine and then 730 mg (2.6 mmol) of 4-benzyloxybenzenesulfonyl chloride in 8 ml of dichloromethane are added to a solution of 800 mg (2.4 mmol) of methyl (S)-3-amino-2-(4-methanesulfonylpiperazin-1-yl)propanoate dihydrochloride in 20 ml of dichloromethane and the reaction medium is stirred at ambient temperature for 3 h. After the addition of water, the product is extracted with dichloromethane. The organic phase is washed with water, dried over magnesium sulfate, filtered and concentrated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08980897B2
Source datasetuspto-grants-2015_03
ORD IDord-858c920c139f46ffbd766fe046cf636a
Source noteuspto-grants-2015_03