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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1264430Generated: October 31, 2026

Ethanol → HCID 86585081, compound

https://huagongshe.com/reaction/1264430

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant1-Ethyl-3-(3'-dimethylaminopropyl)carbodiimideHCID 15908—
ReactantHCID 86585080HCID 86585080—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86585081HCID 8658508134%

Reaction Steps

A suspension of 700 mg (1.29 mmol) (2S,4R)-{[4-Acetylsulfanyl-1-(naphthalene-2-sulfonyl)-pyrrolidine-2-carbonyl]-phenethyl-amino}-acetic acid and 0.1 ml (1.68 mmol) EtOH in 12 ml CH2Cl2 was treated at 0° C. with 273 mg (1.42 mmol) EDCI and 16 mg (0.13 mmol) DMAP. After warming up to RT (1 h), the reaction was partitioned between aqueous 10% KHSO4/Et2O (3×). The organic phases were washed with aqueous saturated KHCO3, 10% NaCl and dried over Na2SO4. Purification by flash-chromatography on silicagel (Hexane/EtOAc 9:1 to 4:1) gave 0.254 mg (34%) (2S,4R)-{[4-Acetylsulfanyl-1-(naphthalene-2-sulfonyl)-pyrrolidine-2-carbonyl]-phenethyl-amino}-acetic acid ethyl ester, mp: 119-120° C., MS: 569 (MH+).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06541638B2
Source datasetuspto-grants-2003_04
ORD IDord-7f7d2781f0fc4f55b6ad9cb2306f7c6a
Source noteuspto-grants-2003_04