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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 704410Generated: November 2, 2026

Dicyclohexylcarbodiimide → 1-[2-(Benzyloxycarbonylamino)-3-hydroxypropionyl]-4-(3-phenylpropyl)piperazine

https://huagongshe.com/reaction/704410

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantN-(Benzyloxycarbonyl)-L-serineHCID 100310—
Reactant1-(3-Phenylpropyl)piperazineHCID 796534—
ReactantHCID 178527226HCID 178527226—
SolventDimethylformamideHCID 6228—
SolventEthyl AcetateHCID 8857—
Product1-[2-(Benzyloxycarbonylamino)-3-hydroxypropionyl]-4-(3-phenylpropyl)piperazineHCID 1488154973.1%

Reaction Steps

Dicyclohexylcarbodiimide (1.58 g) was added to an ice-cooled solution of 2.0 g of N-carbobenzyloxyserine, 1.57 g of 1-(3-phenylpropyl)piperazine and 1.04 g of 1-hydroxybenzotiazole in 30 ml of N,N-dimethylformamide. The mixture was stirred at room temperature for 24 hours, then diluted with ethyl acetate, washed in sequence with two portions of 4% aqueous sodium hydrogen carbonate, one portion of water and one portion of saturated aqueous solution of sodium chloride, dried over anhydrous sodium sulfate and concentrated under reduced pressure. The residue was purified by silica gel column chromatography to give 2.39 g of 1-[2-(benzyloxycarbonylamino)-3-hydroxypropionyl]-4-(3-phenylpropyl}piperazine. Melting point 95°-97° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04987132
Source datasetuspto-grants-1991_01
ORD IDord-3046f51986a644cea6a3ac80c2e3dd47
Source noteuspto-grants-1991_01