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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1266903Generated: October 31, 2026

HCID 18660664, compound → HCID 18660673, compound

https://huagongshe.com/reaction/1266903

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18660664HCID 18660664—
ReactantHydrochloride methanolHCID 21893726—
ProductHCID 18660673HCID 1866067388%

Reaction Steps

Added to 1.3 g of 1-(2-O-(tert-butyldimethylsilyl)-3-C-triphenylsilylethynyl-β-D-ribofuranosyl)uracil obtain above were 30 ml of a 2.6% (w/v) hydrochloric acid/methanol solution, and the mixture was stirred at room temperature. After 110 minutes, the solvent was distilled off under reduced pressure, and the residue was then azeotropically distilled with ethanol, purified by column chromatography on covered silica gel (chloroform:methanol=20:1-15:1) and then suspended in hexane. The suspension was filtered to obtain 940 mg (yield: 86%) of the title compound as a pale-yellow powdered substance.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUSRE038090E1
Source datasetuspto-grants-2003_04
ORD IDord-b9ac2a2bc6bb40788a8f6aba3c6ca848
Source noteuspto-grants-2003_04