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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 653407Generated: October 26, 2026

Piperazine → 4-(Piperazin-1-yl)thieno[3,2-c]pyridine

https://huagongshe.com/reaction/653407

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPiperazineHCID 4837—
Reactant4-Chlorothieno[3,2-c]pyridineHCID 12827312—
SolventEthanolHCID 702—
Product4-(Piperazin-1-yl)thieno[3,2-c]pyridineHCID 1096602756.1%

Reaction Steps

A mixture of 4-chlorothieno[3,2-c]pyridine (22.7 g, 0.13 mole) and piperazine (57.7 g, 0.67 mole) were heated in a bomb with a minimum amount of ethanol (50 mL) at 120° for 24 hours. The reaction was cooled, partitioned between dichloromethane and water, and the organic layer was isolated, dried (MgSO4), filtered, and concentrated in vacuo to an oil. Flash chromatography (methylene chloride-10% methanol-1% ammonium hydroxide) of this material gave 16 g (54%) of a golden oil. Treatment of an ethanol solution of the oil with ethanolic HCl followed by recrystallization from ethanol gave the hydrochloride salt as off-white crystals, m.p. 275°-283°.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04677104
Source datasetuspto-grants-1987_06
ORD IDord-835e7b028b934112bcad12d39be926bf
Source noteuspto-grants-1987_06