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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1633306Generated: October 31, 2026

Dicyclohexylcarbodiimide → HCID 22828235, compound

https://huagongshe.com/reaction/1633306

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(((Tert-butoxy)carbonyl)amino)-3-(4-chlorophenyl)propanoic acidHCID 4164897—
ReactantHCID 54526695HCID 54526695—
SolventWaterHCID 962—
SolventTetrahydrofuranHCID 8028—
ProductHCID 22828235HCID 2282823535.3%

Reaction Steps

A mixture of methyl-1-(6-amino-9H-purin-9-yl)-1,3-dideoxy-3-amino-β-D-ribofuranuronate (294 mg) prepared in Example 62, N-tert-butoxycarbonyl-β-(4-chlorophenyl)-D,L-alanine (300 mg) and N,N'-dicyclohexylcarbodiimide (206 mg) in tetrahydrofuran (15 ml) and water (5 ml) was stirred overnight. The mixture was diluted with water (50 ml) and extracted with ethyl acetate. The extract was washed with water, dried, and evaporated to dryness. The residue was subjected to column chromatography on silica gel. The elution was carried out with a mixed solvent (chloroform/methanol=97/3). The eluate was evaporated to dryness to give methyl 1-(6-amino-9H-purin-9-yl)-1,3-dideoxy-3-[N-tert-butoxycarbonyl-β-(4-chlorophenyl)-D,L-alanylamino]-β-D-ribofuranuronate (203 mg), mp. 120°-125° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04479942
Source datasetuspto-grants-1984_10
ORD IDord-16100e2a11cb4fbab579b8d51d43be9f
Source noteuspto-grants-1984_10