HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-(Quinoxalin-6-yl)-1-(4-(3-(trifluoromethyl)-phenyl)piperidino)ethanone
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | 2-(Quinoxalin-6-yl)acetic acid | HCID 18436916 | — |
| Reactant | 4-(3-Trifluoromethylphenyl)piperidine, HCl | HCID 22252849 | — |
| Catalyst | Benzotriazol-1-yloxy-tris(dimethylamino)phosphonium hexafluorophosphate | HCID 151348 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 2-(Quinoxalin-6-yl)-1-(4-(3-(trifluoromethyl)-phenyl)piperidino)ethanone | HCID 67019198 | 74.6% |
Reaction Steps
0.48 g (2.55 mmol) of quinoxalin-6-ylacetic acid is mixed in 25 ml of DMF, and 1.07 ml of TEA, 0.68 g (2.55 mmol) of 4-(3-(trifluoromethyl)phenyl)piperidine hydrochloride and 1.13 mg of BOP are added thereto. The mixture is heated at ambient temperature overnight, 200 ml of water are added and extraction is carried out with ethyl acetate. The organic phase is dried over sodium sulfate and filtered, and the solvent is evaporated under reduced pressure. A dark oil is thus obtained, which oil is purified by flash chromatography on a column of silica gel, elution being carried out with ethyl acetate. 0.76 g of the title product is obtained in the form of a yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07326720B2 |
| Source dataset | uspto-grants-2008_02 |
| ORD ID | ord-d2042c9196374f709806d9079233e2b5 |
| Source note | uspto-grants-2008_02 |