HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydrochloric Acid → 1-(3,5-Di-O-benzyl-beta-D-Allofuranosyl)Thymine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | 1-(2-O-Acetyl-6-O-Benzoyl-3,5-Di-O-benzyl-beta-D-Allofuranosyl)Thymine | HCID 10555777 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-(3,5-Di-O-benzyl-beta-D-Allofuranosyl)Thymine | HCID 10838010 | — |
Reaction Steps
To a stirred solution of nucleoside 15 (3.00 g, 4.88 mmol) in methanol (50 cm3) was added sodium methoxide (0.79 g, 14.7 mmol). The reaction mixture was stirred for 14 h at room temperature and subsequently neutralised with dilute hydrochloric acid (5 cm3) whereupon ice-cold H2O (50 cm3) was added. The resulting mixture was extracted using ethyl acetate (3×100 cm3) and the combined organic phase was evaporated to dryness under reduced pressure. The residue was purified by silica gel column chromatography using dichloromethane/methanol (98.5:1.5, v/v) as eluent to give nucleoside 16 as white solid material (2.00 g, 88%) after evaporation of the solvents under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07084125B2 |
| Source dataset | uspto-grants-2006_08 |
| ORD ID | ord-a99ac7b5da104cf58c343a9f780e764c |
| Source note | uspto-grants-2006_08 |