HuagongsheHuagongshe Chemistry Print Report · For research reference only
(4-Fluorophenyl)(2-(piperazin-1-yl)pyrimidin-5-yl)methanone → HCID 118023301, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (4-Fluorophenyl)(2-(piperazin-1-yl)pyrimidin-5-yl)methanone | HCID 118022709 | — |
| Reactant | HCID 178461630 | HCID 178461630 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 118023301 | HCID 118023301 | 10% |
Reaction Steps
To a solution of (4-fluorophenyl)(2-(piperazin-1-yl)pyrimidin-5-yl)methanone (4.0 g, 21.84 mmol) in dry THF (150 mL) was added EtMgBr (1 M in THF, 150 mL) at 0° C. under nitrogen. The mixture was stirred at RT for 3 h, then quenched with NH4Cl solution and extracted with ethyl acetate (200*3 mL). The combined organic layers were washed with water and brine, dried over sodium sulfate, filtered and concentrated. The residue was purified by combi-flash with dichloromethane:methanol=10:1 to give the title compound (440 mg, 10%) as a yellow solid. MS (ES+) C17H21FN4O requires: 316. found: 317 [M+H]+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US09200002B2 |
| Source dataset | uspto-grants-2015_12 |
| ORD ID | ord-f5614aa96f1c44d9b8d93709766b96e1 |
| Source note | uspto-grants-2015_12 |