HuagongsheHuagongshe Chemistry Print Report · For research reference only
Diisopropylethylamine → N,N-Dibenzyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 4-Bromopyridine Hydrobromide | HCID 44630127 | — |
| Reactant | (Dibenzyl) [2-(4-piperidyl)ethyl]amine | HCID 66798731 | — |
| Solvent | 1-Butanol | HCID 263 | — |
| Product | N,N-Dibenzyl-2-(1-(pyridin-4-yl)piperidin-4-yl)ethanamine | HCID 66799257 | 53% |
Reaction Steps
N,N-Dibenzyl-2-(piperidin-4-yl)ethanamine (2.4 g, 7.79 mmol, 1 eq) and 4-bromopyridine HBr (1.97 g, 10.12 mmol, 1.3 eq) were dissolved in n-butanol (30 ml) and DIPEA (3.3 ml, 19.47 mmol, 2.5 eq) and the mixture was refluxed for 48 h. After monitoring by thin-layer chromatography, the reaction solution was concentrated under reduced pressure and the residue was taken up in dichloromethane (100 ml), washed with water and sat. NaCl solution (in each case 50 ml), dried over sodium sulfate and concentrated under reduced pressure. After purification by column chromatography (silica gel, 3.5% MeOH in dichloromethane), a white solid was obtained. Yield: 53% (1.6 g, 4.15 mmol).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08680159B2 |
| Source dataset | uspto-grants-2014_03 |
| ORD ID | ord-46feede4f6bd453f891f58330bae694d |
| Source note | uspto-grants-2014_03 |