HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 178473802, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 178478641 | HCID 178478641 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Potassium bisulfate | HCID 516920 | — |
| Product | HCID 178473802 | HCID 178473802 | 72.2% |
Reaction Steps
To a stirring solution of 3-[5-(4-fluorophenyl)-4-pyridin-4-yl-1H-imidazol-2-yl]piperidine dihydrochloride (0.76 mmol, 0.3 g) in THF (5.0 mL) was added triethylamine (3.3 mmol, 0.33 g) and acetyl chloride (2.3 mmol, 0.18 g). The reaction was stirred at room temperature for 1H, diluted with 10% KHSO4 (50 mL) and extracted with ethyl acetate (2×50 mL). The organics were combined, washed with brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was chromatographed over silica, eluting with 3% MeOH:CH2Cl2. The pure fractions were collected and evaporated under reduced pressure. The resulting film was evaporated from CH2Cl2 :hexanes to give 0.2 g of the title compound as a white foam.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06083949 |
| Source dataset | uspto-grants-2000_07 |
| ORD ID | ord-a90049b7027b420a879500816858e3ee |
| Source note | uspto-grants-2000_07 |