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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 733196Generated: October 30, 2026

Water → 4-(2-Chloro-5-(trifluoromethyl)phenyl)-6-propylpyrimidine-2-carbonitrile

https://huagongshe.com/reaction/733196

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
Reactant2-Chloro-5-(trifluoromethyl)phenylboronic acidHCID 2782670—
Reactant4-Iodo-6-propyl-pyrimidine-2-carbonitrileHCID 86619638—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventTolueneHCID 1140—
Product4-(2-Chloro-5-(trifluoromethyl)phenyl)-6-propylpyrimidine-2-carbonitrileHCID 4986242258%

Reaction Conditions

Temperature105 °C

Reaction Steps

Under nitrogen atmosphere, a solution (c=0.18 M) of 4-iodo-6-propyl-pyrimidine-2-carbonitrile (1 mL, 0.18 mmol) in degassed toluene, an aqueous solution (c=2 M) of potassium carbonate (0.225 mL, 0.45 mmol) and tetrakis(triphenylphosphine) palladium (10 mg, 0.09 mmol) were successively added to a solution (c=0.216 M) of 2-chloro-5-(trifluoromethyl)phenyl boronic acid (1 ml, 0.216 mmol) in degassed toluene. The mixture was heated at 105° C. for 4 h, then was allowed to cool to room temperature and mixed with water (4 mL). The organic layer was evaporated under reduced pressure. The residue was chromatographed by preparative HPLC (H2O+0.05% TFA/CH3CN+0.05% TFA) to afford 4-(2-chloro-5-trifluoromethyl-phenyl)-6-propyl-pyrimidine-2-carbonitrile (34 mg, 58%) as a solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07589095B2
Source datasetuspto-grants-2009_09
ORD IDord-da720f3f061c4bad80b59edcf116d58d
Source noteuspto-grants-2009_09