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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 347721Generated: October 30, 2026

Dimethylformamide → HCID 58801101, compound

https://huagongshe.com/reaction/347721

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-Nitrophenyl chloroformateHCID 82129—
ReactantMethyl 2-(S)-[N-carbobenzyloxy]amino-3-aminopropionate, hydrochlorideHCID 13756825—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductHCID 58801101HCID 58801101—

Reaction Conditions

Temperature25 °C

Reaction Steps

To a solution of the compound of Reference Example 13 (300 mg) and ethyldiisopropylamine (0.656 ml) in dichloromethane (10 ml) is added chloroformic acid p-nitrophenyl ester (273 mg), and the mixture is stirred at 25° C. for 6 hours. To the reaction solution are added a solution of (2S)-3-amino-2-(benzyloxycarbonylamino)propanoic acid methyl ester hydrochloride (709 mg) and ethyldiisopropylamine (0.65 ml) in dimethylformamide (20 ml), and the mixture is stirred at 60° C. overnight. The reaction solution is diluted with ethyl acetate, and then the mixture is washed successively with 10% aqueous citric acid solution, saturated aqueous sodium hydrogen carbonate solution, and saturated brine, dried over magnesium sulfate, and the solvent is evaporated under reduced pressure. The residue is purified by silica gel column chromatography (eluent: gradient, 0% to 100% ethyl acetate/hexane) to give the title compound (120 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07176199B2
Source datasetuspto-grants-2007_02
ORD IDord-7c41607a6f0b49038136f0efa8933284
Source noteuspto-grants-2007_02