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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2207849Generated: October 25, 2026

2-Chloroquinoline → 2-(3-((3-(Tetrahydro-2H-pyran-4-YL)pyridin-2-YL)oxy)azetidin-1-YL)quinoline

https://huagongshe.com/reaction/2207849

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-ChloroquinolineHCID 11928—
ReactantBinap, (A+-)-HCID 634876—
ReactantSodium t-butoxideHCID 23676156—
Reactant2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyridineHCID 58547765—
CatalystBis(dibenzylideneacetone)palladiumHCID 9811564—
SolventTolueneHCID 1140—
Product2-(3-((3-(Tetrahydro-2H-pyran-4-YL)pyridin-2-YL)oxy)azetidin-1-YL)quinolineHCID 5854791010%

Reaction Conditions

Temperature130 °C

Reaction Steps

A mixture of 2-(azetidin-3-yloxy)-3-(tetrahydro-2H-pyran-4-yl)pyridine (see PREPARATION P27.1; 100 mg, 0.45 mmol), 2-chloroquinoline (73 mg, 0.45 mmol), Pd2(dba)3 (56 mg, 0.062 mmol), 2,2′-bis(diphenylphosphino)-1,1′-binaphthyl (BINAP) (40 mg, 0.06 mmol), KI (40 mg, 0.13 mmol) and sodium tert-butoxide (t-BuONa) (110 mg, 1.2 mmol) was dissolved in toluene (5 mL). The reaction mixture was heated in a microwave at 130° C. for 4 hours. The solvent was evaporated and the crude product was purified by silica gel column chromatography to give the product (6.7 mg, 0.018 mmol, yield 10%). [M+1] 363. IC50 (uM) 0.331.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09376450B2
Source datasetuspto-grants-2016_06
ORD IDord-7d4cb9b8ed49418e94bd8513c2931a37
Source noteuspto-grants-2016_06