HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 18660664, compound → HCID 18660673, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 18660664 | HCID 18660664 | — |
| Reactant | Hydrochloride methanol | HCID 21893726 | — |
| Product | HCID 18660673 | HCID 18660673 | 88% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | USRE038090E1 |
| Source dataset | uspto-grants-2003_04 |
| ORD ID | ord-b9ac2a2bc6bb40788a8f6aba3c6ca848 |
| Source note | uspto-grants-2003_04 |