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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 261066Generated: October 27, 2026

Benzene → 6-Chloro-2-(4-cyclopropylmethyl-1-piperazinyl)-pyrazine hydrochloride

https://huagongshe.com/reaction/261066

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzeneHCID 241—
ReactantHydrochloric AcidHCID 313—
Reactant6-Chloro-2-(4-cyclopropanecarbonyl-1-piperazinyl)-pyrazineHCID 20396001—
SolventDiethyl EtherHCID 3283—
SolventIsopropanol ethanolHCID 22179027—
Product6-Chloro-2-(4-cyclopropylmethyl-1-piperazinyl)-pyrazine hydrochlorideHCID 20396014—

Reaction Steps

To a stirred slurry of 3.0 g (11 mmol) of the product from the previous step in 30 ml dry ether is added 5.5 ml of a 70% benzene solution of sodium bis-2-methoxyethoxyaluminum hydride at -20° C. under N2. The temperature of the mixture is raised to +10° C. for 20 minutes and the mixture is recooled to -20° C. and treated dropwise with 33 ml 4 N aqueous hydrochloric acid. The aqueous acid layer is extracted with chloroform, adjusted to pH8 with sodium bicarbonate and the crude title base extracted with chloroform and chromatographed on silica gel. Elution with ethylacetatechloroform gives fractions containing 0.8 g (29%) of pure title base which is converted to the hydrochloride, mp 254° C. dec in ethanol-isopropanol containing hydrochloric acid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04163849
Source datasetuspto-grants-1979_08
ORD IDord-475abd387ef8447196e09d27c3cb3083
Source noteuspto-grants-1979_08