HuagongsheHuagongshe Chemistry Print Report · For research reference only
Carbon Tetrachloride → 5-Amino-1-(5-chloro-5-deoxy-beta-d-ribofuranosyl)imidazole-4-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Carbon Tetrachloride | HCID 5943 | — |
| Reactant | Triphenylphosphine | HCID 11776 | — |
| Reactant | Triphenylphosphine Oxide | HCID 13097 | — |
| Reactant | Acadesine | HCID 17513 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Amino-1-(5-chloro-5-deoxy-beta-d-ribofuranosyl)imidazole-4-carboxamide | HCID 53796407 | — |
Reaction Steps
AICA riboside (1.00 g), triphenylphosphine (3.05 g) and carbon tetrachloride (1.15 ml) were stirred in dimethyl formamide (38 ml) at room temperature for 3 hours. The solution was diluted with methanol (15 ml), then concentrated under reduced pressure. The resulting yellow tar was chromatographed on silica gel, eluting with 4:1 methylene chloride:methanol. The like fractions were combined and concentrated under reduced pressure to afford a purple foam. The presence of triphenylphosphine oxide, as determined by 1H NMR, necessitated a second chromotographic step as above. Yield was 0.43 g of a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08993527B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-4e69ce4502574a80b09210e4e467c79f |
| Source note | uspto-grants-2015_03 |