HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 1-Acetyl-4-(4,6-difluoropyrimidin-2-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,4,6-Trifluoropyrimidine | HCID 69677 | — |
| Reactant | 1-Acetylpiperazine | HCID 83795 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 1-Acetyl-4-(4,6-difluoropyrimidin-2-yl)piperazine | HCID 18423050 | — |
| Product | 1-Acetyl-4-(2,6-difluoropyrimidin-4-yl)piperazine | HCID 18423152 | — |
Reaction Steps
To a solution of 2,4,6-trifluoropyrimidine (2.0 g) and potassium carbonate (3.1 g) in acetonitrile (15 ml) was added a solution of 1-acetylpiperazine (1.9 g) in acetonitrile (5 ml) over 10 min under ice-cooling and the mixture was stirred at room temperature for 1 hr. The reaction mixture was poured into water and extracted with ethyl acetate. The extract was washed with brine and dried over anhydrous sodium sulfate. The solvent was evaporated to give a pale-yellow oil. The obtained pale-yellow oil was purified by silica gel column chromatography to give the title compound (1.8 g) and 1-acetyl-4-(2,6-difluoropyrimidin-4-yl)piperazine (1.7 g) both as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06455528B1 |
| Source dataset | uspto-grants-2002_09 |
| ORD ID | ord-b2048bc1cd7a4f399b5faa32651e1386 |
| Source note | uspto-grants-2002_09 |