HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-(16,17-Dihydroxyheptadecyl)-3,7-dimethylxanthine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Sodium Sulfite | HCID 24437 | — |
| Reactant | Methyl morpholine oxide | HCID 82029 | — |
| Reactant | 1-(16-Heptadecenyl)-3,7-dimethylxanthine | HCID 23295936 | — |
| Solvent | Acetone water tetrahydrofuran | HCID 21553975 | — |
| Product | 1-(16,17-Dihydroxyheptadecyl)-3,7-dimethylxanthine | HCID 23435630 | 81% |
Reaction Steps
A solution of 1-(16-Heptadecenyl)-3,7-dimethylxanthine (1.50 g, 3.60 mmol), 4-methylmorpholine-N-oxide (1.83 mL, 60% wt in water, 10.6 mmol) and potassium osmate dihydrate (16 mg, 0.04 mmol) in acetone/water/ tetrahydrofuran (10:7:5, 110 mL) was stirred for 60 hours. Water (100 mL) and sodium sulfite (1 g) were added and the reaction mixture stirred for 1 hour. The reaction mixture was extracted with dichloromethane (2×100 mL) and the organic phase dried using magnesium sulfate and the solvent evaporated to afford a cream solid. Recrystallization from hot ethyl acetate yields 1.31 g (81% yield) of 1-(16,17-dihydroxyheptadecyl)-3,7-dimethylxanthine (inventive compound no. 3514).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866576 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-2df91c9668b14d34989866dcbb8964ae |
| Source note | uspto-grants-1999_02 |