HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dichloromethane → {3-[5-(4-Methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanol
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Sodium Sulfate | HCID 24436 | — |
| Reactant | Diisobutylaluminumhydride | HCID 21225700 | — |
| Reactant | Methyl 3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]-benzoate | HCID 59484904 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | {3-[5-(4-Methylpiperazin-1-yl)pyrimidin-2-yl]phenyl}methanol | HCID 59484860 | — |
Reaction Steps
860 mg (2.75 mmol) of methyl 3-[5-(4-methylpiperazin-1-yl)pyrimidin-2-yl]-benzoate are dissolved in 16 ml of THF, and 13.8 ml (13.8 mmol) of 1 M diisobutylaluminium hydride in THF are added dropwise at room temperature, and the reaction mixture is stirred at room temperature for 1 h. A further 13.8 ml 13 (13.8 mmol) of 1 M diisobutylaluminium hydride in THF are added dropwise, and the reaction mixture is stirred at room temperature for 1 h. 3 ml of saturated sodium sulfate solution are added to the reaction mixture with ice-cooling. Dichloromethane is added to the gelatinous mixture, which is then stirred for 30 min and filtered. The filtrate is dried over sodium sulfate and evaporated.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08435986B2 |
| Source dataset | uspto-grants-2013_05 |
| ORD ID | ord-a70b9c3c6e214e779f67b133edb67521 |
| Source note | uspto-grants-2013_05 |