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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1733470Generated: November 1, 2026

Piperazine → HCID 20299635, compound

https://huagongshe.com/reaction/1733470

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
ReactantHCID 20299638HCID 20299638—
SolventAcetonitrileHCID 6342—
ProductHCID 20299635HCID 20299635—

Reaction Steps

6-Chloro-3-trifluoromethylthioimidazo[1,2-a]pyrazine from Step A is reacted with piperazine (2 g) in efluxing acetonitrile for 24 hours. The mixture is cooled, concentrated under vacuum, and the esidue partitioned between dilute sodium hydroxide and chloroform. The chloroform extract is dried over sodium sulfate, filtered and concentrated under vacuum to the crude base which is purified by chromatography on silica gel and converted to 6-(1-piperazinyl)-3-trifluoromethylthioimidazo[1,2-a]pyrazine hydrochloride with ethanolic hydrogen chloride.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04242344
Source datasetuspto-grants-1980_12
ORD IDord-7524e5751b054103995019081c48b783
Source noteuspto-grants-1980_12