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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1761398Generated: October 31, 2026

110714-14-2 → HCID 14551079, compound

https://huagongshe.com/reaction/1761398

Reaction equation

Participants

RoleNameHCIDCharge
Reactant110714-14-2HCID 14551076—
ReactantN-Benzyl-2-chloro-N-(2-phenoxyethyl)ethan-1-amine--hydrogen chloride (1/1)HCID 14551077—
SolventEthanolHCID 702—
SolventSodiumHCID 5360545—
ProductHCID 14551079HCID 1455107980.5%

Reaction Steps

2.43 g (0.015 mole) of 6-(1-imidazolyl)-3(2H)-pyridazinone are dissolved in the solution of 0.35 g (0.015 g-atom) of sodium in 12 ml of absolute ethanol and the solution is stirred at room temperature for 15 minutes. To the thus-obtained suspension, the base liberated from the solution of 4.89 g (0.015 mole) of N-(2-chloroethyl)-N-(2-phenoxyethyl)-N-benzylamine hydrochloride [dissolved in 12 ml of absolute ethanol by adding a solution of 0.35 g (0.015 g-atom) of sodium in 12 ml of absolute ethanol] is added, thereupon the mixture is stirred at room temperature for 30 minutes and then boiled under reflux while stirring for 4 hours, set aside overnight at room temperature and evaporated. The residue is taken up in 200 ml of chloroform, filtered, the organic solution is washed with water, dried and evaporated under reduced pressure. The residue weighing 5.82 g is dissolved in absolute acetone and a calculated amount of ethanolic hydrogen chloride solution is added, diluted with isopropanol and kept in the refrigerator overnight. The precipitate is filtered off, washed with acetone and dried to give 5.9 g (80% yield) of the aimed product, m. p. 153°-156° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04826845
Source datasetuspto-grants-1989_05
ORD IDord-612512b0cb114b33bad4c8b9189f900d
Source noteuspto-grants-1989_05