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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1613491Generated: November 1, 2026

Benzenesulfonyl chloride → HCID 178472453, compound

https://huagongshe.com/reaction/1613491

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzenesulfonyl chlorideHCID 7369—
ReactantTriethylamineHCID 8471—
ReactantHCID 178472452HCID 178472452—
SolventDichloromethaneHCID 6344—
ProductHCID 178472453HCID 17847245374%

Reaction Steps

2-Amino-3-{1-[(cis-4-ethoxycarbonyl-cyclohexyl)carbamoyl]-cyclopentyl}propanoic acid t-butyl ester (0.605 g, 1.48 mmole) was dissolved in dry dichloromethane (25 ml) and treated at 0° C. with triethylamine (0.45 g, 4.4 mmole) and benzene sulphonyl chloride (0.24 ml, 1.84 mmole). After stirring for 16 hours at room temperature under nitrogen the dichloromethane was removed under vacuum, the residue taken up in diethyl ether (25 ml), washed with dilute hydrochloric acid, dilute sodium hydrogen carbonate and water, dried (Na2SO4) and the solvent evaporated under vacuum to give the crude product. Purification by column chromatography on silica, eluting with diethyl etherdichloromethane mixtures, gave pure title compound as a white foam (0.60 g, 74%). Found: C,61.38; H,7.85; N,5.06. C28H42N2O7S requires C,61.06; H,7.69; N,5.09%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05192800
Source datasetuspto-grants-1993_03
ORD IDord-cd56313061f840d891626cee359576ed
Source noteuspto-grants-1993_03