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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 526450Generated: October 30, 2026

1,4-Dioxane → N-cyclopropyl-N-methylazetidin-3-amine

https://huagongshe.com/reaction/526450

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,4-DioxaneHCID 31275—
ReactantTert-butyl 3-(cyclopropyl(methyl)amino)azetidine-1-carboxylateHCID 117601211—
SolventHydrochloric AcidHCID 313—
SolventDichloromethaneHCID 6344—
ProductN-cyclopropyl-N-methylazetidin-3-amineHCID 62783698—

Reaction Conditions

Temperature20 °C

Reaction Steps

Combine a solution of tert-butyl 3-(cyclopropyl(methyl)amino)azetidine-1-carboxylate (73 mg, 0.323 mmol) in methylene chloride (3 mL) and 4 M HCl in dioxane (0.323 mL, 1.290 mmol) and the solution stirred at 20° C. for 4 hours then added 4 M HCl in dioxane (0.323 mL, 1.290 mmol) and stirred at 20° C. for 21 h. The solution was then concentrated in vacuo to give the title compound as a hydrochloride salt which was used without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09345713B2
Source datasetuspto-grants-2016_05
ORD IDord-b97d483b9e6346e58f5ba983330d3e1e
Source noteuspto-grants-2016_05