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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2202184Generated: October 31, 2026

Water → Benzyl 4-[2-(4-hydroxybenzenesulfonylamino)-1-methoxycarbonylethyl]piperazine-1-carboxylate

https://huagongshe.com/reaction/2202184

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
Reactant4-Hydroxybenzene-1-sulfonyl chlorideHCID 11424093—
ReactantBenzyl 4-(2-amino-1-methoxycarbonylethyl)piperazine-1-carboxylate dihydrochlorideHCID 86675018—
SolventDichloromethaneHCID 6344—
ProductBenzyl 4-[2-(4-hydroxybenzenesulfonylamino)-1-methoxycarbonylethyl]piperazine-1-carboxylateHCID 7111550846%

Reaction Conditions

Temperature0 °C

Reaction Steps

2.1 ml (15 mmol) of triethylamine and then 920 mg (5 mmol) of 4-hydroxybenzenesulfonyl chloride in 20 ml of dichloromethane are added dropwise to a solution of 1.1 g (3 mmol) of benzyl 4-(2-amino-1-methoxycarbonylethyl)piperazine-1-carboxylate dihydrochloride in 30 ml of dichloromethane, cooled beforehand to 0° C. The reaction medium is then stirred at ambient temperature for 18 h. After the addition of water, the reaction medium is extracted with dichloromethane. The organic phase is with water and then dried over magnesium sulfate, filtered and concentrated under vacuum. The crude residue obtained is purified by chromatography on silica gel, elution being carried out with a 50/50 heptane/ethyl acetate mixture. 60 mg (46%) of benzyl 4-[2-(4-hydroxybenzenesulfonylamino)-1-methoxycarbonylethyl]piperazine-1-carboxylate are obtained in the form of a white solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09365529B2
Source datasetuspto-grants-2016_06
ORD IDord-9e6341abd51547c2aa99190f8528bfec
Source noteuspto-grants-2016_06