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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966338Generated: October 30, 2026

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

https://huagongshe.com/reaction/1966338

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 DMF (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 confirmed 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 numberUS08420653B2
Source datasetuspto-grants-2013_04
ORD IDord-0a346fb59ff0466d8eb47a7d2c4c48fe
Source noteuspto-grants-2013_04