HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → Isopropyl purine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | 2-Chloro-9-isopropyl-N-(4-methoxybenzyl)-9H-purin-6-amine | HCID 9858785 | — |
| Reactant | 2-Chloro-N-(4-methoxybenzyl)-9H-purin-6-amine | HCID 16422056 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Isopropyl purine | HCID 18473604 | 89% |
Reaction Steps
Preparation of 2-chloro-6-(4-methoxybenzylamino)-9-isopropylpurine (2) The 6-(4-methoxybenzylamino)-2-chloropurine (496 mg, 1.7 mmol) was suspended in dry DMF (5 ml) and treated with sodium hydride, 60% dispersion (82 mg, 2.06 mmol). The suspension was stirred for 30 min over which time it became a clear yellow/green solution. 2-Iodopropane (0.280 mL, 1.7 eq.) was added over 5 min and the resultant solution stirred for 2 days. Water was added and the solution and extracted with ethyl acetate. The organic layer was evaporated to give the product isopropyl purine (508 mg, 89%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05866702 |
| Source dataset | uspto-grants-1999_02 |
| ORD ID | ord-04655bddf1e441ed9ea634d9d34ca14a |
| Source note | uspto-grants-1999_02 |