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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454947Generated: October 29, 2026

Hydrochloride methanol → 2-(3-((5-(Piperidin-4-yl)pyrimidin-4-yl)oxy)azetidin-1-yl)quinoline hydrochloride

https://huagongshe.com/reaction/454947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloride methanolHCID 21893726—
ReactantTert-butyl 4-(4-((1-(quinolin-2-YL)azetidin-3-YL)oxy)pyrimidin-5-YL)piperidine-1-carboxylateHCID 58547690—
Product2-(3-((5-(Piperidin-4-yl)pyrimidin-4-yl)oxy)azetidin-1-yl)quinoline hydrochlorideHCID 67477416—

Reaction Steps

The mixture of tert-butyl 4-(4-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrimidin-5-yl)piperidine-1-carboxylate (307 mg, 0.66 mmol) in HCl/MeOH (10 mL, saturated with HCl gas) was stirred at room temperature for 1 hour. Then it was concentrated to give 2-(3-((5-(piperidin-4-yl)pyrimidin-4-yl)oxy)azetidin-1-yl)quinoline hydrochloride which was used in the next step below without further purification.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497265B2
Source datasetuspto-grants-2013_07
ORD IDord-e74dcf261cd84e40aa3deb60c6d75442
Source noteuspto-grants-2013_07