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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 232193Generated: October 29, 2026

Dicyclohexylcarbodiimide → HCID 67902445, compound

https://huagongshe.com/reaction/232193

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant1-HydroxybenzotriazoleHCID 75771—
ReactantHCID 14181639HCID 14181639—
Reactant5-[(4-Nitrophenyl)methoxy]-4,5-dioxopentanoateHCID 22166415—
SolventDichloromethaneHCID 6344—
ProductHCID 67902445HCID 6790244575.7%

Reaction Steps

In 3 ml of dichloromethane were dissolved 85 mg of the Compound (1) obtained in Example 1 and 41 mg of 1-hydroxybenzotriazole (HOBT). To the solution was added 62 mg of DCC, and the mixture was stirred at room temperature for 30 minutes, to which was added 60 mg of (4R)-4-benzyloxycarbonylamino-3-isoxazolidinone, prepared by the method described in Journal of Medicinal Chemistry, 13 1013 (1970), followed by stirring at room temperature for 30 minutes. The insolubles which separated out were filtered off and washed with dichloromethane. The filtrate and the washing were combined and concentrated. The concentrate was dissolved in ethyl acetate. The solution was washed with an aqueous solution of sodium hydrogen carbonate and a saturated saline, successively, which was then dried (Na2SO4). The solvent was evaporated off under reduced pressure, and the residue was subjected to a silica gel column chromatography, followed by elution with hexane-ethyl acetate (1:1) to give 96 mg of the subject compound (8) as colorless foamy substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04851422
Source datasetuspto-grants-1989_07
ORD IDord-96f3f44a44ac4db781f05275bf97cf67
Source noteuspto-grants-1989_07