Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2113630Generated: November 1, 2026

Potassium Carbonate → 6-Methyl-3'-trifluoromethyl-[2,2']bipyridinyl-5-carbonitrile

https://huagongshe.com/reaction/2113630

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1,4-DioxaneHCID 31275—
ReactantMethylboronic AcidHCID 139377—
Reactant6-Chloro-3'-trifluoromethyl-[2,2']bipyridinyl-5-carbonitrileHCID 58628189—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product6-Methyl-3'-trifluoromethyl-[2,2']bipyridinyl-5-carbonitrileHCID 58628191—

Reaction Conditions

Temperature115 °C

Reaction Steps

In a sealed tube, dissolve 6-chloro-3′-trifluoromethyl-[2,2′]bipyridinyl-5-carbonitrile (242 mg, 0.853 mmol), CH3B(OH)2 (300 mg, 5.10 mmol), K2CO3 (1.6 g, 12 mmol), and Pd(PPh3)4 in a solution of dioxane (10 mL) and H2O (2 mL). Bubble argon through the mixture for 30 minutes and seal. Heat the mixture at 115° C. overnight. Cool the mixture to room temperature. Add H2O (20 mL) and extract with EtOAc (3×20 mL). Combine the organic extracts and wash with brine (60 mL). Dry the organic layer over Na2SO4 and remove the solvent under reduced pressure. Purify the crude product using silica gel chromatography eluting with EtOAc/hexane (1:1) to yield the title compound. MS 264.07 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07432275B2
Source datasetuspto-grants-2008_10
ORD IDord-6fee241b24664faa8a6bba38cc01b94c
Source noteuspto-grants-2008_10