Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Xanthine | HCID 1188 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 547768 | HCID 547768 | — |
| Reactant | 3-Methyl-7-propylpurine-2,6-dione | HCID 3314397 | — |
| Reactant | Potassium | HCID 5462222 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 13747693 | HCID 13747693 | — |
Reaction Steps
A solution of 5.6 g (0.1 mol) of potassium hydroxide in 100 ml of methanol is added to a suspension of 20.8 g (0.1 mol) of 3-methyl-7-propylxanthine in 250 ml of methanol. On heating, a clear solution forms, and this is evaporated to dryness under reduced pressure. The potassium salt of the xanthine compound which remains is intensively dried under a high vacuum, 500 ml of dimethylformamide and 15.0 g (0.11 mol) of the tertiary alcohol from stage (a) are added and the mixture is stirred at 80° C. for 18 hours. The mixture is worked up analogously to Example 5b, whereupon 25.1 g of crude product (81.4% of theory) are obtained and can be purified by recrystallization from diisopropyl ether, with the addition of a little ethyl acetate, at the boiling point.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04833146 |
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| Source dataset | uspto-grants-1989_05 |
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| ORD ID | ord-ed6f1a9bfef74ccaa75f4f79a9ba3e94 |
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| Source note | uspto-grants-1989_05 |
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