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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354305Generated: November 2, 2026

Dicyclohexylcarbodiimide → HCID 86628795, compound

https://huagongshe.com/reaction/2354305

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDicyclohexylcarbodiimideHCID 10868—
Reactant2-(Benzyloxy) ethanolHCID 12141—
ReactantHCID 57616312HCID 57616312—
Catalyst4-(Dimethylamino)pyridineHCID 14284—
SolventDichloromethaneHCID 6344—
ProductHCID 86628795HCID 8662879541.3%

Reaction Steps

To a mixture of 3-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-1-[4-((1E)-3-carboxyprop-1-enyl)benzyl]-7-methyl-1H-indole (0.10 g), 2-(benzyloxy)ethanol (22 mg), 4-dimethylaminopyridine (7 mg) and dichloromethane (0.5 mL) was added dicyclohexylcarbodiimide (37 mg), and the mixture was stirred at room temperature overnight. The reaction mixture was directly purified by column chromatography on silica gel (eluent: n-hexane/ethylacetate=4/1-2/1) to give 3-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-1-(4-{(1E)-3-[2-(benzyl-oxy)ethoxycarbonyl]prop-1-enyl}benzyl)-7-methyl-1H-indole (48 mg). This material was dissolved in a mixed solvent of methanol (1 mL) and tetra hydrofuran (1 mL). To the solution was added 10% palladium-carbon powder (50 mg), and the mixture was stirred at room temperature under a hydrogen atmosphere for 4 hours. The insoluble material was removed by filtration, and the solvent was removed under reduced pressure. The residue was purified by column chromatography on silica gel (eluent: dichloromethane/methanol=12/1-8/1) to give the title compound (14 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750145B2
Source datasetuspto-grants-2010_07
ORD IDord-80978ab070054139a6cd8e2d400ca0a5
Source noteuspto-grants-2010_07