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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1657784Generated: November 1, 2026

Pyridine → HCID 21388469, compound

https://huagongshe.com/reaction/1657784

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
Reactant1-(Chloroacetyl)pyrrolidineHCID 88440—
ReactantHCID 21388458HCID 21388458—
ReactantHCID 21388459HCID 21388459—
SolventBenzeneHCID 241—
ProductHCID 21388469HCID 21388469—

Reaction Steps

To 17.7 g. of N-(α-cyano-3,4-dimethoxybenzyl)piperazine was added 60 ml. of benzene and then 5.3 g. of pyridine. To the resulting solution was added dropwise 7.9 g. of pyrrolidylcarbonylmethyl chloride dissolved in 20 ml. of benzene over a period of about 10 minutes with stirring at room temperature. After dropping, the temperature was raised slowly and the mixture to separate benzene layer which was washed with water and dried over sodium sulfate. The solvent was distilled off to give 15 g. of N-(α-cyano-3,4-dimethoxybenzyl)-N'-pyrrolidinocarbonylmethylpiperazine as an oily substance. This product was dissolved in benzene and the resultant solution was saturated with dry hydrochloric gas to separate crystal which was collected by filtration. Recrystallization from iso-propanol afforded N-(α-cyano-3,4-dimethoxybenzyl)-N'-pyrrolidinocarbonylmethylpiperazine hydrochloride monohydrate having a melting point of 155° to 157°C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS03962247
Source datasetuspto-grants-1976_06
ORD IDord-778ea1434f78432b854d9e1180a96768
Source noteuspto-grants-1976_06