HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → 3-[(Phenylcarbonyl)amino]-N-(tetrahydrofuran-2-ylmethyl)-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-(Isocyanatomethyl)oxolane | HCID 18467517 | — |
| Reactant | ethyl-N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamide | HCID 66701258 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 3-[(Phenylcarbonyl)amino]-N-(tetrahydrofuran-2-ylmethyl)-5-[4-(trifluoromethyl)phenyl]piperidine-1-carboxamide | HCID 66701526 | — |
Reaction Steps
80 mg (0.23 mmol) of ethyl-N-{5-[4-(trifluoromethyl)phenyl]piperidin-3-yl}benzamide were initially charged in 2 ml of THF, and 29 mg (0.23 mmol) of 2-(isocyanatomethyl)tetrahydrofuran and 35 μl (0.25 mmol) of triethylamine were added. The mixture was stirred at RT overnight. The reaction mixture was then purified by preparative HPLC (Reprosil C18, water/acetonitrile gradient). Yield: 88 mg (81% of theory)
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08987248B2 |
| Source dataset | uspto-grants-2015_03 |
| ORD ID | ord-d8691db52196442faf14f6edeac930dd |
| Source note | uspto-grants-2015_03 |