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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 251417Generated: November 2, 2026

Potassium Carbonate → 4,5-Diphenyl-6-(4-pyridin-2-yl-piperazin-1-yl)-2-(trifluoromethyl)pyrimidine

https://huagongshe.com/reaction/251417

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-(2-Pyridyl)piperazineHCID 94459—
Reactant4-Chloro-5,6-diphenyl-2-(trifluoromethyl)pyrimidineHCID 10404680—
SolventDimethylformamideHCID 6228—
Product4,5-Diphenyl-6-(4-pyridin-2-yl-piperazin-1-yl)-2-(trifluoromethyl)pyrimidineHCID 2495902669.66%

Reaction Conditions

Temperature28 °C

Reaction Steps

To a solution of 4-chloro-5,6-diphenyl-2-(trifluoromethyl)pyrimidine (0.5 g, 1.49 mmol, prepared according to the procedure described in PCT/IB03/02879) in dimethylformamide (5 ml) was added 1-pyridin-2-yl piperazine (0.107 g, 0.66 mmol) and anhydrous potassium carbonate (0.2 g) under stirring at 28° C. The reaction mixture was stirred for 4 hours and when TLC conformed the completion, it was poured onto ice. The solid thus obtained was filtered and washed with water (20 ml). The above solid was then dissolved in dichloromethane (50 ml) and dried over anhydrous sodium sulphate. Evaporation of the solvent afforded the title compound (0.48 g, yield 69.66%, purity by HPLC 99.8%). m.p. 165-167° C. 1H-NMR (CDCl3) δ: 3.43 (s, 8H), 6.58-6.64 (m, 2H), 7.14-7.21 (m, 7H), 7.26-7.29 (m, 3H), 7.45-7.49 (t, 1H), 8.14-8.15 (d, 1H). IR cm−1 (KBr): 3436, 2839, 1591, and 1557. MS m/z: 462.1 (M++1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07863446B2
Source datasetuspto-grants-2011_01
ORD IDord-169caa3c7c6849d4adc7fceaaa246f71
Source noteuspto-grants-2011_01