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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1834068Generated: November 1, 2026

Pyridine → HCID 21388469, compound

https://huagongshe.com/reaction/1834068

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. Recrystrallization 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 numberUS04068070
Source datasetuspto-grants-1978_01
ORD IDord-1386b6dc03884f6c92338685412027d2
Source noteuspto-grants-1978_01