HuagongsheHuagongshe Chemistry Print Report · For research reference only
Acetyl chloride → HCID 21101584, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | HCID 21101591 | HCID 21101591 | — |
| Catalyst | 4-(Dimethylamino)pyridine | HCID 14284 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 21101584 | HCID 21101584 | — |
Reaction Steps
2-tert-Butoxycarbonylamino-7-chloro-4-[4-(4-fluorophenylaminocarbonyl)piperazin-1-yl]quinoline (110 mg, 0.22 mmol) in CH2Cl2 (1 mL) is treated with trifluoroacetic acid (1 mL) for 2 h at room temp. The reaction mixture is concentrated. The residue is dissolved in CH2Cl2 (9 mL). Triethylamine (154 μL, 1.1 mmol), acetyl chloride (26 μL, 0.24 mmol), and DMAP (10 mg) are added. The reaction mixture is stirred at room temp. for 3 h, washed with water, dried (MgSO4), and concentrated. Purification of the residue by column chromatography with CH2Cl2-MeOH affords the title product.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-cb5c99020b25409db45bcba40c79d419 |
| Source note | uspto-grants-2007_05 |