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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1057028Generated: November 2, 2026

Potassium Carbonate → 2-((6-methyl-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrile

https://huagongshe.com/reaction/1057028

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantMethylboronic AcidHCID 139377—
Reactant2-((6-chloro-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrileHCID 72550713—
CatalystHCID 178477754HCID 178477754—
Product2-((6-methyl-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrileHCID 725507149%

Reaction Conditions

Temperature100 °C

Reaction Steps

A vial was charged with 2-[(6-chloro-4-tetrahydropyran-4-yl-2-pyridyl)amino]pyridine-4-carbonitrile (51.1 mg, 0.162 mmol), [1,1-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (13.5 mg, 10 mol %), methylboronic acid (20.0 mg, 0.325 mmol), and potassium carbonate (68 mg, 0.49 mmol) and purged under nitrogen before the addition of degassed 1,4-dioxane (1.6 mL) and degassed water (0.5 mL). The mixture was stirred at 100° C. for 19 hr and then diluted with CH2Cl2, filtered through Celite and washed with brine. The organics were dried over MgSO4 and concentrated to dryness. The reaction residue thus obtained was purified by RPLC to afford 2-((6-methyl-4-(tetrahydro-2H-pyran-4-yl)pyridin-2-yl)amino)isonicotinonitrile as a white solid (4.1 mg, 9%); ESI-LRMS m/z [M+1]+=295.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09399636B2
Source datasetuspto-grants-2016_07
ORD IDord-f8571fe90a7e4f1ebacfd68d05be7f97
Source noteuspto-grants-2016_07