Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2354304Generated: November 1, 2026

Hydrochloric Acid → HCID 86628794, compound

https://huagongshe.com/reaction/2354304

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium IodideHCID 5238—
ReactantCesium carbonateHCID 10796—
ReactantBenzene, ((2-bromoethoxy)methyl)-HCID 73833—
ReactantHCID 57616421HCID 57616421—
SolventDimethylformamideHCID 6228—
ProductHCID 86628794HCID 8662879494.9%

Reaction Steps

A suspension of 3-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-1-(4-carboxybenzyl)-7-methyl-1H-indole (90 mg), benzyl 2-bromoethyl ether (37 mg), cesium carbonate (74 mg) and sodium iodide (3 mg) in N,N-dimethylformamide (1 mL) was stirred at room temperature for 1 day. The reaction mixture was poured into 0.5 mol/L hydrochloric acid, and the resulting mixture was extracted with ethylacetate. The extract was washed with water and brine successively, and dried over anhydrous sodium sulfate. The solvent was removed under reduced pressure, and the residue was purified by column chromatography on silica gel (eluent: n-hexane/ethyl acetate=3/1-3/2) to give 3-(2,3,4,6-tetra-O-benzyl-β-D-glucopyranosyl)-1-{4-[2-(benzyloxy)ethoxycarbonyl]benzyl}-7-methyl-1H-indole (0.10 g). This material was dissolved in a mixed solvent of methanol (2 mL) and tetra hydrofuran (2 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=8/1-5/1) to give the title compound (42 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07750145B2
Source datasetuspto-grants-2010_07
ORD IDord-e30159d7f59a43db954ed725e482d1c3
Source noteuspto-grants-2010_07