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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 266373Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 53735824, compound

https://huagongshe.com/reaction/266373

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantEthyl 3-aminobenzoateHCID 11400—
ReactantHCID 178448385HCID 178448385—
SolventDichloromethaneHCID 6344—
ProductHCID 53735824HCID 5373582449.8%

Reaction Steps

The procedure described in Example 180 was repeated, except that (S)-2-(4-bromobenzenesulfonylamino)-4-methylthiobutanoic acid (2.99 g) and ethyl 3-aminobenzoate (1.34 g) were condensed in dichloromethane (100 ml) in the presence of N,N'-dicyclohexylcarbodiimide (2.01 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-(3-ethoxycarbonylphenyl)-4-methylthiobutanamide (2.018 g).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05650428
Source datasetuspto-grants-1997_07
ORD IDord-6dcbaa8a97ed446a8189d1455fe8e2d2
Source noteuspto-grants-1997_07