HuagongsheHuagongshe Chemistry Print Report · For research reference only
Triethylamine → N-(1-Benzylpiperidin-4-yl)[1,1'-biphenyl]-2-carboxamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Benzyl-4-piperidylamine | HCID 415852 | — |
| Reactant | 4'-(Trifluoromethyl)-[1,1'-biphenyl]-2-carbonyl chloride | HCID 11066000 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | N-(1-Benzylpiperidin-4-yl)[1,1'-biphenyl]-2-carboxamide | HCID 15135612 | — |
Reaction Steps
3 g (0.014 mol) of 4′-trifluoromethyl-biphenyl-2-carboxylic acid chloride, dissolved in 30 ml of dichloromethane, are added dropwise at 15 to −20° C. to a solution of 2.65 ml (0.013 mol) of 4-amino-1-benzyl-piperidine and 6 ml (0.043 mol) of triethylamine in 100 ml of dichloromethane. The mixture is stirred for 14 hours at ambient temperature. The reaction solution is extracted with a mixture of I molar sodium hydrogen carbonate solution and 1N sodium hydroxide solution. The organic phase is dried over sodium sulphate and the solvent is eliminated. The residue is recrystallised from 650 ml of ethanol.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06617325B1 |
| Source dataset | uspto-grants-2003_09 |
| ORD ID | ord-de8dfeeff7404ce8808f4a0d384d2ce9 |
| Source note | uspto-grants-2003_09 |