HuagongsheHuagongshe Chemistry Print Report · For research reference only
Methanol → Hypoxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | HCID 9914306 | HCID 9914306 | — |
| Reactant | HCID 21998625 | HCID 21998625 | — |
| Catalyst | Nickel | HCID 935 | — |
| Solvent | 1-Propanol | HCID 1031 | — |
| Product | Hypoxanthine | HCID 135398638 | 35.1% |
Reaction Steps
3-(3-Benzyloxy-4-methoxy-benzyl)-8-(1-benzyloxy-1-methyl-ethyl)-2-thioxanthine (26.05 g, 48 mmole) was heated under reflux in 1-propanol (700 ml) with Raney-nickel (29 g) (treated with 0.1% aqueous acetic acid) for 1.5 hours. The nickel was filtered off and the solvent evaporated in vacuo. The residue was dissolved in dichloromethane (300 ml), extracted with sodium carbonate solution and evaporated again to dryness. The residue was dissolved in methanol (150 ml), treated with charcoal, filtered, concentrated and crystallized to give 3-(3-benzyloxy-4-methoxy-benzyl)-8-(1-benzyloxy-1-methyl-ethyl)-hypoxanthine (15.81 g, 64.5%), mp 78-86° C. (containing methanol). A second crop gave 2.29 g (9.3%) of hypoxanthine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06228859B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-5e4d8350c5b64a86a59dbb3ab0e03367 |
| Source note | uspto-grants-2001_05 |