HuagongsheHuagongshe Chemistry Print Report · For research reference only
6-Chlorohexan-2-one → 7-Benzyl-3-methyl-1-(5-oxohexyl)xanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 6-Chlorohexan-2-one | HCID 82468 | — |
| Reactant | 7-Benzyl-3-methylxanthine | HCID 685630 | — |
| Product | 7-Benzyl-3-methyl-1-(5-oxohexyl)xanthine | HCID 20041127 | 90.4% |
Reaction Steps
The compound was also accessible, inter alia, by first reacting 7-benzyl-3-methylxanthine with 1-chloro-5-hexanone under the reaction conditions described above to give 7-benzyl-3-methyl-1-(5-oxohexyl)-xanthine (yield 90.4% of theory, melting point: 82°-84° C.) and then reductively methylating the oxohexyl side chain with methylmagnesium chloride in anhydrous ether analogously to Example 9 (yield: 60.2% of theory; melting point: 108°-110° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04833146 |
| Source dataset | uspto-grants-1989_05 |
| ORD ID | ord-f6ab901c84be423b84344d8dcc200b81 |
| Source note | uspto-grants-1989_05 |