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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266369Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 54388403, compound

https://huagongshe.com/reaction/266369

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
ReactantHCID 178448387HCID 178448387—
SolventDichloromethaneHCID 6344—
ProductHCID 54388403HCID 543884032.1%

Reaction Steps

The procedure described in Example 180 was repeated, except that (R)-2-(4-chlorobenzenesulfonylamino)-4-methylthiobutanoic acid (715 mg) and ethyl 4-aminophenylacetate (430 mg) were condensed in dichloromethane (15 ml) in the presence of N,N'-dicyclohexylcarbodiimide (546 mg). The reaction mixture was filtered, and the filtrate was concentrated. The resulting crude product was recrystallized from hexanechloroform to obtain (R)-2-(4-chlorobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-methylthiobutanamide (22.9 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650428
Source datasetuspto-grants-1997_07
ORD IDord-25bb722662bd4e25b8a0f520c01f590c
Source noteuspto-grants-1997_07