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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2278457Generated: October 27, 2026

Sodium Carbonate → cis-2-[2-(2,6-Dimethyl-4-morpholinyl)-5-(2-methyl-4-pyridinyl)-4-pyrimidinyl]-6-(trifluoromethyl)benzonitrile hydrochloride

https://huagongshe.com/reaction/2278457

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant2-(5,5-Dimethyl-1,3,2-dioxaborinan-2-yl)-6-(trifluoromethyl)benzonitrileHCID 11623335—
Reactantcis-4-(4-Chloro-5-(2-methylpyridin-4-yl)pyrimidin-2-yl)-2,6-dimethylmorpholineHCID 86702425—
CatalystDichlorobis(triphenylphosphine)palladiumHCID 6102075—
SolventWaterHCID 962—
Solvent1,2-DimethoxyethaneHCID 8071—
Productcis-2-[2-(2,6-Dimethyl-4-morpholinyl)-5-(2-methyl-4-pyridinyl)-4-pyrimidinyl]-6-(trifluoromethyl)benzonitrile hydrochlorideHCID 8670243548.8%

Reaction Conditions

Temperature100 °C

Reaction Steps

Sodium carbonate (166 mg, 1.568 mmol) in water (2 mL), bis(triphenylphosphine) palladium(II) chloride (11.01 mg, 0.016 mmol) and 2-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-6-(trifluoromethyl)benzonitrile (178 mg, 0.627 mmol) were added to a solution of cis-4-[4-chloro-5-(2-methyl-4-pyridinyl)-2-pyrimidinyl]-2,6-dimethylmorpholine (100 mg, 0.314 mmol) in 1,2-dimethoxyethane (3 mL). The reaction mixture was heated to 100° C. for 2 hours. The reaction mixture diluted with water (5 mL) and extracted with DCM (5 mL×2). The organic extracts were combined, dried (MgSO4), filtered and the solvent was removed. The resulting residues were then purified by MDAP and fractions containing desired product were combined and evaporated to dryness. The solid was dissolved in methanol (2 mL) and 4M HCl in dioxane (1 mL) was added. The solvent was removed to give the title compound (75 mg). LC/MS [M+H]+=454.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09133178B2
Source datasetuspto-grants-2015_09
ORD IDord-10b17b55eade4ffc9d6640b205e451cd
Source noteuspto-grants-2015_09