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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266372Generated: October 30, 2026

Dicyclohexylcarbodiimide → HCID 53793533, compound

https://huagongshe.com/reaction/266372

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactantp-Aminophenylacetic acid ethyl esterHCID 225219—
ReactantHCID 178448385HCID 178448385—
SolventDichloromethaneHCID 6344—
ProductHCID 53793533HCID 5379353316%

Reaction Steps

The procedure described in Example 180 was repeated, except that (S)-2-(4-bromobenzenesulfonylamino)-4-methylthiobutanoic acid (7.86 g) and ethyl 4-aminophenylacetate (3.64 g) were condensed in dichloromethane (80 ml) in the presence of N,N'-dicyclohexylcarbodiimide (5.28 g). The reaction mixture was filtered, and the filtrate was concentrated. The resulting crude product was recrystallized from ethanol to obtain (S)-2-(4-bromobenzenesulfonylamino)-N-(4-(ethoxycarbonylmethyl)phenyl)-4-methylthiobutanamide (1.67 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650428
Source datasetuspto-grants-1997_07
ORD IDord-d04e09b40038496db6988977302c61cd
Source noteuspto-grants-1997_07