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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1651552Generated: November 2, 2026

Hydrazine → HCID 15055857, compound

https://huagongshe.com/reaction/1651552

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrazineHCID 9321—
Reactant1H-Isoindole-1,3(2H)-dione, 2-(2-bromoethyl)-HCID 11325—
ReactantPotassium CarbonateHCID 11430—
ReactantSodium HydroxideHCID 14798—
Reactant2-((4-Chlorophenyl)(4-piperidinyloxy)methyl)pyridineHCID 11141197—
SolventEthanolHCID 702—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 15055857HCID 1505585741%

Reaction Steps

7.50 g (24.77 mmol) of 4-[(4-chlorophenyl)-2-pyridylmethoxy]piperidine and 6.92 g (27.24 mmol) of N-(2-bromoethyl)phthalimide were dissolved in 60 ml of dioxane, and 4.11 g (29.74 mmol) of potassium carbonate was added. The mixture was stirred at an oil bath temperature of 90° to 100° C. for 3 hours. After the reaction, the insolubles were filtered off, and the filtrate was concentrated under reduced pressure. The residue was separated by silica gel column chromatography using a mixture of ethyl acetate and methanol in the volume ratio 25:1 as an eluent. The desired fraction was concentrated under reduced pressure, and 60 ml of ethanol and 1.61 g (32.16 mmol) of hydrazine (hydrate) were added to the residue, and the mixture was stirred under reflux. After 200 ml of 1N aqueous sodium hydroxide was added to the reaction mixture, the mixture was extracted twice with 200 ml of chloroform. The chloroform extract was dried over anhydrous sodium sulfate and concentrated under reduced pressure to give 3.50 g (41%) of 2-[4-[(4-chlorophenyl)-2-pyridylmethoxy]-1-piperidyl]ethylamine as an oily product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04929618
Source datasetuspto-grants-1990_05
ORD IDord-c476f6c0deb44775ab78a4283595b55a
Source noteuspto-grants-1990_05