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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1195675Generated: October 26, 2026

Hydrochloric Acid → 1-[2-(Benzofurazan-5-yl)ethyl]-4-(benzofurazan-5-carbonyl)piperidine hydrochloride

https://huagongshe.com/reaction/1195675

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantSodium BicarbonateHCID 516892—
Reactant5-(2-Bromoethyl)benzofurazanHCID 11775899—
Reactant4-(Benzofurazan-5-carbonyl)piperidine hydrochlorideHCID 67916351—
CatalystLithium iodideHCID 66321—
SolventEthanolHCID 702—
SolventEthyl AcetateHCID 8857—
Product1-[2-(Benzofurazan-5-yl)ethyl]-4-(benzofurazan-5-carbonyl)piperidine hydrochlorideHCID 6791634440.3%

Reaction Steps

4-(Benzofurazan-5-carbonyl)piperidine hydrochloride (80 mg, 0.3 mmol), 5-(2-bromoethyl)benzofurazan (170 mg, 0.75 mmol), sodium bicarbonate (101 mg, 1.2 mmol) and lithium iodide (1 mg) in ethanol were heated under reflux for 19 hours, cooled and the solvent was evaporated under reduced pressure. The residue was purified by flash column chromatography on silica gel, eluting with CH2Cl2 /CH3OH/NH3 (Aq.); 98:2:0.2 to give a yellow solid. This was dissolved in ethyl acetate (2 ml), and ethanolic HCl (Ca. 1M, 1 ml) was added. The resulting solid was collected and dried in vacuo to give the hydrochloride as a white solid (50 mg, 40%), mp 226°-228° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05112824
Source datasetuspto-grants-1992_05
ORD IDord-2148e4ced9f7442b85c974b23b1e804c
Source noteuspto-grants-1992_05