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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1251323Generated: November 3, 2026

Pyridine → HCID 18323651, compound

https://huagongshe.com/reaction/1251323

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-(2-Methoxyphenyl)piperazineHCID 1346—
Reactant6-Bromohexanoyl chlorideHCID 89848—
SolventDichloromethaneHCID 6344—
ProductHCID 18323651HCID 1832365176.1%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06342498B1
Source datasetuspto-grants-2002_01
ORD IDord-53add0ddece845e19405d7b9fac9c0f1
Source noteuspto-grants-2002_01