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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1061033Generated: November 3, 2026

Bromide ion → HCID 22709662, compound

https://huagongshe.com/reaction/1061033

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBromide ionHCID 259—
ReactantTriethylamineHCID 8471—
ReactantSodium AcetateHCID 517045—
ReactantHCID 11398144HCID 11398144—
SolventEthanolHCID 702—
ProductHCID 22709662HCID 22709662—

Reaction Steps

In ethanol, 1-[(6-chloronaphthalen-2-yl)sulfonyl]-4-[(4,5,6,7-tetrahydrothieno[3,2-c]pyridin-2-yl)carbonyl]piperazine hydrochloride (195 mg), triethylamine (0.2 ml) and sodium acetate (118 mg) were suspended, followed by the addition of cyan bromide (114 mg). The resulting mixture was stirred at room temperature for 2 hours. The residue obtained by concentrating the reaction mixture under reduced pressure was added with dichloromethane, followed by washing with water. After drying over anhydrous sodium sulfate, the residue obtained by distilling off the solvent under reduced pressure was purified by chromatography on a silica gel column (dichloromethane:methanol=100:1), whereby the title compound (51 mg, 28%) was obtained.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06525042B1
Source datasetuspto-grants-2003_02
ORD IDord-141902c71e484d4ab1b6e2ec954e898c
Source noteuspto-grants-2003_02