HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → 1-((4-Chlorophenyl)(1-methylpiperidin-4-yl)methyl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-(Chloro(4-chlorophenyl)methyl)-1-methylpiperidine | HCID 59716933 | — |
| Solvent | Methyl Ethyl Ketone | HCID 6569 | — |
| Product | 1-((4-Chlorophenyl)(1-methylpiperidin-4-yl)methyl)piperazine | HCID 59716937 | 62% |
Reaction Steps
A mixture of 4-(chloro(4-chlorophenyl)methyl)-1-methylpiperidine (1.2 g, 4.66 mmol) in butanone (10 ml), anhydrous piperazine (1.58 g, 18.45 mmol), anhydrous K2CO3 (0.63 g, 4.61 mmol) and KI (0.76 g, 4.61 mmol) was refluxed under nitrogen for 18 hours. The mixture was then cooled and filtered and the solvent removed in vacuo. The residue was dissolved in CH2Cl2 (50 ml) and washed with water (30 ml). Drying and removal of the solvent followed by chromatography (CH2Cl2:CH3OH:NH4OH 90:10:0.5) afforded desired product in 62% yield.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07649092B2 |
| Source dataset | uspto-grants-2010_01 |
| ORD ID | ord-f074183e4eaa49f182a017430131d006 |
| Source note | uspto-grants-2010_01 |