HuagongsheHuagongshe Chemistry Print Report · For research reference only
Isopropyl iodide → 5-Iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Isopropyl iodide | HCID 6362 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | 5-Iodo-7H-pyrrolo[2,3-d]pyrimidine | HCID 10610336 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-Iodo-7-isopropyl-7H-pyrrolo[2,3-d]pyrimidine | HCID 70817176 | 77% |
Reaction Steps
To a mixture of 5-iodo-7H-pyrrolo[2,3-d]pyrimidine (Preparation 201, 2.90 g, 12.0 mmol) and cesium carbonate (5.78 g, 17.8 mmol) in DMF (45 mL) was added 2-iodopropane (1.78 mL, 17.8 mmol). The mixture was stirred at room temperature for 3 hours. The reaction mixture was then poured onto saturated aqueous ammonium chloride (500 mL) and a solid precipitated. The solid was collected by filtration, rinsed with water (200 mL) and dried under reduced pressure for 17 hours to afford the title compound as a brown solid in 77% yield, 2.61 g.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08846698B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-62c92f0c8c86496cb5550895e0d2c83d |
| Source note | uspto-grants-2014_09 |