HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium citrate, potassium citrate, citric acid → 4-azidoacetyl-1-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)-5-(dimethylaminomethyleneamino)imidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium citrate, potassium citrate, citric acid | HCID 171403 | — |
| Reactant | Sodium Methoxide | HCID 10942334 | — |
| Reactant | 1-(3,5-di-O-acetyl-2-deoxy-2-fluoro-beta-D-ribofuranosyl)-4-azidoacetyl-5-(dimethylaminomethyleneamino)imidazole | HCID 54278308 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-azidoacetyl-1-(2-deoxy-2-fluoro-beta-D-ribofuranosyl)-5-(dimethylaminomethyleneamino)imidazole | HCID 54402470 | 60% |
Reaction Steps
The compound (22) (130 mg) obtained in item (11) above was dissolved in methanol (6 ml), to which was added a 0.2M sodium methylate solution (0.5 ml) in methanol and the resulting mixture was allowed to stand at room temperature for 30 minutes. The reaction solution as formed was neutralized with addition of ion-exchange resin, Amberlite CG-120 (H+ form) (100-200 mesh), filtered and the filtrate was concentrated to give a solid material which was then washed with diethylether to afford the titled compound (23) (63 mg) as an insoluble substance. Yield: 60%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05773607 |
| Source dataset | uspto-grants-1998_06 |
| ORD ID | ord-c5894fee5415438d9993ce76ab956ba8 |
| Source note | uspto-grants-1998_06 |