HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → 5,6-Dichloro-1-(2-deoxy-2-fluoro-3,5-diacetyl-beta-D-ribofuranosyl)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | 5,6-Dichloro-1-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)benzimidazole | HCID 10663538 | — |
| Product | 5,6-Dichloro-1-(2-deoxy-2-fluoro-3,5-diacetyl-beta-D-ribofuranosyl)benzimidazole | HCID 70287888 | 98% |
Reaction Conditions
| Temperature | 0 °C |
|---|
Reaction Steps
Compound 15 (0.45 g, 1.4 mmol) was dissolved in pyridine (20 mL) and boiled to remove water. The solution was chilled to 0° C. in an ice bath. Acetic anhydride (260 μL, 2.9 mmol, 2 equiv.) was added and the reaction mixture was allowed to warm to room temperature while stirring overnight. Methanol (3 mL) was added and the solvents removed in vacuo. Residual pyridine was removed by coevaporation with toluene (3×). The residue was partitioned between water and the ethyl acetate. The ethyl acetate solution was dried with magnesium sulfate, filtered, and the solvent removed in vacuo to yield 0.56 g (98%) of compound 16. The product was used without further purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05840743 |
| Source dataset | uspto-grants-1998_11 |
| ORD ID | ord-9a97f5a9f3564ec7bc7ac5a6b666c4ad |
| Source note | uspto-grants-1998_11 |