HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 9-(3-Bromopropyl)-2-butoxy-8-methoxy-9H-purin-6-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 1,3-Dibromobutane | HCID 7889 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-(Butyloxy)-8-(methyloxy)-9H-purin-6-amine | HCID 57457134 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 9-(3-Bromopropyl)-2-butoxy-8-methoxy-9H-purin-6-amine | HCID 23158490 | 71% |
Reaction Steps
To a solution of 2-butoxy-8-methoxyadenine (5 g, 14.2 mmol) in dimethylformamide (50 ml) were added 1,3-dibromobutane (7.2 ml) and potassium carbonate (9.2 g), and the mixture was stirred at room temperature for 1.5 hour. Water (200 ml) and ethyl acetate (75 ml) were added thereto, and the mixture was extracted, and further extracted with ethyl acetate (75 ml) twice. The organic layers were combined, dried over magnesium sulfate, filtered, and the solvent was distilled off under reduced pressure. To the residue was added diethyl ether (25 ml), and the precipitated crystals were collected by filtration, washed with ether (5 ml), and dried to give the subtitle compound (3.6 g) as a white solid. Yield: 71%
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08044056B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-aeb930831a124e69ad5924a36ad1318d |
| Source note | uspto-grants-2011_10 |