HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline → HCID 178523789, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Chloro-6-fluoro-2-(trifluoromethyl)quinoline | HCID 2736591 | — |
| Reactant | N-(4-aminocyclohexyl)-3,5-difluorobenzamide | HCID 22641525 | — |
| Solvent | N-methyl-2-pyrrolidone | HCID 13387 | — |
| Product | HCID 178523789 | HCID 178523789 | — |
Reaction Steps
A solution of N-(4-Amino-cyclohexyl)-3,5-difluorobenzamide (30 mg, 0.12 mmol) in NMP (1.0 mL) was treated with 4-chloro-6-fluoro-2-trifluoromethyl-quinoline (1 eq) and 3 eq (0.045 mL) TEA. The reaction was heated to 220 C in the microwave for 15 minutes. The crude compound was purified by reverse phase HPLC to provide the desired compound. MS (ESI (+)) m/e 468 (M+H)+; 1H NMR (500 MHz, DMSO) δ ppm 8.32 (m, 2 H), 7.98 (m, 1 H), 7.67 (m, 1 H), 7.58 (m, 2 H), 7.44 (m, 1 H), 7.15 (d, 1 H), 6.82 (s, 1 H), 1.95 (m, 4 H), 1.65-1.88 (m, 4 H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06818772B2 |
| Source dataset | uspto-grants-2004_11 |
| ORD ID | ord-4787ccb1b4b842df84cd8b6cab01970f |
| Source note | uspto-grants-2004_11 |