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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1378452Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 10552575, compound

https://huagongshe.com/reaction/1378452

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantHOAtHCID 181649—
Reactant1-Sulfanylcyclopentane-1-carboxylic acidHCID 15817584—
ReactantHCID 86749398HCID 86749398—
SolventDichloromethaneHCID 6344—
SolventTriethylamineHCID 8471—
ProductHCID 10552575HCID 10552575—

Reaction Steps

To a stirred solution of 1-mercapto-1-cyclopentanecarboxylic acid (1.74 g, 4.54 mmol) in dichloromethane (50 mL) and triethylamine (0.63 mL) is added [(1-amino-(1-cyclopentyl)carbonyl]-L-tyrosine butyl ester hydrochloride (0.66 g). To this solution is added 1-hydroxy-7-azabenzotriazole (0.68 g, 4.55 mmol) and 1,3-dicyclohexylcarbodiimide (1.03 g, 4.99 mmol). The mixture is stirred for 14 hours and then the solid precipitate is removed by filtration. The organic phase is washed with a saturated solution of sodium bicarbonate (10 mL), brine (10 mL), dried over magnesium sulfate and the solvent is removed to give a clear oil. The oil is purified by flash chromatography (SiO2, hexane/ethyl acetate, 6:4) to give a clear foam. The foam is crystallized from ethyl ether to yield N-[[1-[[(1-mercapto-1-cyclopentyl)carbonyl]amino]-1-cyclopentyl]carbonyl]-L-tyrosine butyl ester, m.p. 106°-107° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05668158
Source datasetuspto-grants-1997_09
ORD IDord-e5e927817a2744be940cd68c5d7fc6c7
Source noteuspto-grants-1997_09