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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378943Generated: October 30, 2026

Sodium Acetate → 5-(4-Fluorophenyl)-7-(4-imidazol-2-ylpiperidyl)thiopheno[3,2-b]pyridine

https://huagongshe.com/reaction/378943

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium AcetateHCID 517045—
Reactant7-Chloro-5-(4-fluorophenyl)thieno[3,2-b]pyridineHCID 15487432—
Reactant4-(1H-imidazol-2-yl)piperidine hydrochlorideHCID 18465193—
SolventEthylene GlycolHCID 174—
SolventEthyl AcetateHCID 8857—
Product5-(4-Fluorophenyl)-7-(4-imidazol-2-ylpiperidyl)thiopheno[3,2-b]pyridineHCID 990779318%

Reaction Conditions

Temperature160 °C

Reaction Steps

A mixture of 7-chloro-5-(4-fluorophenyl)thieno[3,2-b]pyridine (146 mg, 0.53 mmol), 4-(1H-imidazol-2-yl)piperidine. hydrochloride (U.S. Pat. No. 4,431,653) (100 mg, 0.53 mmole) and sodium acetate (50 mg) in ethylene glycol (10 mL) is stirred and heated at 160° C. for about 16 hours. It is then cooled, diluted with ethylacetate (15 mL), and washed with water (3×15 mL). The organic layer is dried over sodium sulfate, filtered, and concentrated. The residue is purified by preparative thin layer chromatography to give 5-(4-fluorophenyl)-7-(4-imidazol-2-ylpiperidyl)thiopheno[3,2-b]pyridine (36 mg, 18% yield) as a white solid, m.p. 95° C. (compound 1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06297256B1
Source datasetuspto-grants-2001_10
ORD IDord-72a49192428048808f259b5fc31ce228
Source noteuspto-grants-2001_10