HuagongsheHuagongshe Chemistry Print Report · For research reference only
p-Fluorophenethylamine → HCID 21101940, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | p-Fluorophenethylamine | HCID 4653 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | HCID 21101706 | HCID 21101706 | — |
| Product | HCID 21101940 | HCID 21101940 | — |
Reaction Steps
4-[4-(tert-Butoxycarbonyl)piperazin-1-yl]-7-chloroquinol-2-one (150 mg, 0.41 mmol), sodium hydride (15 mg, 0.6 mmol), N-phenyl(trifluoromethylsulfon)imide (208 mg, 0.58 mmol), and 4-fluorophenethylamine (0.22 mL, 1.65 mmol) are treated according to method E yielding 4-[4-(butoxycarbonyl)piperazin-1-yl]-7-chloro-2-[2-(4-fluorophenyl)ethylamino]quinoline, which is deprotected with TFA in CH2Cl2 and transformed into the title product according to method C using 4-fluorophenyl isocyanate (18 μL, 0.16 mmol) and triethylamine (110 μL, 0.79 mmol) to give a colorless solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07220856B2 |
| Source dataset | uspto-grants-2007_05 |
| ORD ID | ord-e8adc4381ae14ecab7c31b37df3109b8 |
| Source note | uspto-grants-2007_05 |