HuagongsheHuagongshe Chemistry Print Report · For research reference only
7-Benzyl-3-methylxanthine → A 802715
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 7-Benzyl-3-methylxanthine | HCID 685630 | — |
| Reactant | 3-Methyl-7-propylpurine-2,6-dione | HCID 3314397 | — |
| Reactant | 3-Methyl-1-(5-methyl-4-hexenyl)-7-propylxanthine | HCID 20041128 | — |
| Product | A 802715 | HCID 129959 | — |
Reaction Steps
The same compound was obtained, inter alia, by alkylation of the compound of Example 6 with 1-bromo- or 1-chloropropane analogously to Example 3, by reaction of 3-methyl-7-propylxanthine with the tertiary alcohol of Example 1a analogously to Example 2, or by acid-catalyzed hydration of 3-methyl-1-(5-methyl-4-hexenyl)-7-propylxanthine analogously to Example 14 below.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04833146 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-bad931619c524789b8a38274bc82424e |
| Source note | uspto-grants-1989_05 |