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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454946Generated: October 29, 2026

Tert-butyl 4-(2-chloro-4-((1-(quinolin-2-YL)azetidin-3-YL)oxy)pyrimidin-5-YL)-5,6-dihydropyridine-1(2H)-carboxylate → Tert-butyl 4-(4-((1-(quinolin-2-YL)azetidin-3-YL)oxy)pyrimidin-5-YL)piperidine-1-carboxylate

https://huagongshe.com/reaction/454946

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTert-butyl 4-(2-chloro-4-((1-(quinolin-2-YL)azetidin-3-YL)oxy)pyrimidin-5-YL)-5,6-dihydropyridine-1(2H)-carboxylateHCID 58547741—
CatalystPalladiumHCID 23938—
SolventMethanolHCID 887—
ProductTert-butyl 4-(4-((1-(quinolin-2-YL)azetidin-3-YL)oxy)pyrimidin-5-YL)piperidine-1-carboxylateHCID 5854769078%

Reaction Steps

To a solution of tert-butyl 4-(2-chloro-4-((1-(quinolin-2-yl)azetidin-3-yl)oxy)pyrimidin-5-yl)-5,6-dihydropyridine-1(2H)-carboxylate (472 mg, 0.95 mmol) in MeOH (10 mL) was added Pd/C (10%, 200 mg). The reaction solution was stirred at room temperature overnight under H2 atmosphere. The mixture was filtered through CELITE® and concentrated to give the product (307 mg, 0.66 mmol, yield: 78%). ESI-MS (M+1): 462 calc. for C26H31N5O3 461.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08497265B2
Source datasetuspto-grants-2013_07
ORD IDord-160e494d300b4823bb2a61f540fce122
Source noteuspto-grants-2013_07