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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1757760Generated: October 28, 2026

Dicyclohexylcarbodiimide → N2 [3(S)-[N-(benzyloxycarbonyl)-L-asparaginylamino]-2(R)-hydroxy-4-phenylbutyl]-N1-tert.butyl-4(R)-hydroxy-L-prolinamide

https://huagongshe.com/reaction/1757760

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
ReactantBenzyloxycarbonyl-asparagineHCID 75314—
ReactantHCID 86746268HCID 86746268—
ReactantHCID 178418300HCID 178418300—
SolventMethanolHCID 887—
SolventDiethyl EtherHCID 3283—
SolventDichloromethaneHCID 6344—
SolventEthyl AcetateHCID 8857—
ProductN2 [3(S)-[N-(benzyloxycarbonyl)-L-asparaginylamino]-2(R)-hydroxy-4-phenylbutyl]-N1-tert.butyl-4(R)-hydroxy-L-prolinamideHCID 8674626637.7%

Reaction Steps

In a manner analogous to that described in Example 92, from 0.133 g of N-(benzyloxycarbonyl)-L-asparagine, 0.068 g of hydroxybenzotriazole, 0.103g of dicyclohexylcarbodiimide and 0.16 g of N2 -[3(S)-amino-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-4(R)-hydroxy-L-prolinamide, but using dichloromethane in placeof ethyl acetate as the partitioning solvent and 20% methanol in dichloromethane for the chromatography and carrying out the re-evaporationwith diethyl ether, there was obtained 0.1 g of N2 -[3(S)-[N-(benzyloxycarbonyl)-L-asparaginylamino]-2(R)-hydroxy-4-phenylbutyl]-N1 -tert.butyl-4(R)-hydroxy-L-prolinamide of melting point 115° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05446161
Source datasetuspto-grants-1995_08
ORD IDord-ddc7a85f60b94842b49c302d52f12498
Source noteuspto-grants-1995_08