HuagongsheHuagongshe Chemistry Print Report · For research reference only
1,4-Dioxane hydrochloride → Phenyl[2-(1-piperazinyl)-5-pyrimidinyl]methanone hydrochloride
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1,4-Dioxane hydrochloride | HCID 20443148 | — |
| Reactant | Tert-butyl 4-(5-benzoylpyrimidin-2-yl)piperazine-1-carboxylate | HCID 118022456 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | Phenyl[2-(1-piperazinyl)-5-pyrimidinyl]methanone hydrochloride | HCID 118022636 | 90% |
Reaction Steps
To a solution of tert-butyl 4-(5-benzoylpyrimidin-2-yl)piperazine-1-carboxylate (1 g, 2.7 mmol) in dioxane (20 mL) was added 4 M HCl-dioxane (20 mL), and the reaction mixture was stirred at room temperature overnight. LCMS showed the reaction was completed. The mixture was directly concentrated to give phenyl(2-(piperazin-1-yl)pyrimidin-5-yl)methanone HCl salt as a yellowish solid (0.95 g, 90%). MS (ES+) C15H16N4O requires: 268, found: 269 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09334263B2 |
| Source dataset | uspto-grants-2016_05 |
| ORD ID | ord-99c7400e40b640e8bd6222be1b684379 |
| Source note | uspto-grants-2016_05 |