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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266375Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 54316364, compound

https://huagongshe.com/reaction/266375

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
ReactantHCID 178446060HCID 178446060—
SolventDichloromethaneHCID 6344—
ProductHCID 54316364HCID 5431636431.4%

Reaction Steps

The procedure described in Example 180 was repeated, except that (S)-2-(4-chlorobenzenesulfonylamino)-4-ethylthiobutanoic acid (695.2 mg) and ethyl 4-aminophenylacetate (380 mg) were condensed in dichloromethane (30 ml) in the presence of N,N'-dicyclohexylcarbodiimide (509.5 mg). The reaction mixture was filtered, and the filtrate was concentrated. The resulting crude product was recrystallized from ethanol to obtain (S)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-ethylthiobutanamide (321.5 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650428
Source datasetuspto-grants-1997_07
ORD IDord-cb8364d6ded943d6bab2e34b8515b689
Source noteuspto-grants-1997_07