HuagongsheHuagongshe Chemistry Print Report · For research reference only
Pyridine → HCID 18323651, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Pyridine | HCID 1049 | — |
| Reactant | 1-(2-Methoxyphenyl)piperazine | HCID 1346 | — |
| Reactant | 6-Bromohexanoyl chloride | HCID 89848 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18323651 | HCID 18323651 | 76.1% |
Reaction Steps
To a stirred mixture of 1-(2-methoxyphenyl)piperazine (21.34 mmol) and pyridine (25.6 mmol) in 60 mL of dry dichloromethane was added dropwise a solution of 6-bromohexanoyl chloride (23.52 mmol) in 20 mL of dichloromethane at 0° C. under nitrogen. After addition, the mixture was allowed to warm to room temperature and stirred for 1-2 hours. The mixture was quenched with 10% potassium carbonate in water, and extracted with dichloromethane. The organic phase was washed with brine and water, dried over magnesium sulfate, filtered and concentrated. The residue was purified by flash chromatography using 5% methanol, 0.5% ammonium hydroxide in ethyl acetate to give 1-(2-methoxyphenyl)-4-(6-bromohexanoyl)piperazine (6.00 g, 76%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06342498B1 |
| Source dataset | uspto-grants-2002_01 |
| ORD ID | ord-53add0ddece845e19405d7b9fac9c0f1 |
| Source note | uspto-grants-2002_01 |