HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354305Generated: November 2, 2026
Dicyclohexylcarbodiimide → HCID 86628795, compound
https://huagongshe.com/reaction/2354305
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dicyclohexylcarbodiimide | HCID 10868 | — |
| Reactant | 2-(Benzyloxy) ethanol | HCID 12141 | — |
| Reactant | HCID 57616312 | HCID 57616312 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 86628795 | HCID 86628795 | 41.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07750145B2 |
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| Source dataset | uspto-grants-2010_07 |
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| ORD ID | ord-80978ab070054139a6cd8e2d400ca0a5 |
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| Source note | uspto-grants-2010_07 |
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