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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 220531Generated: October 26, 2026

Potassium Carbonate → 4-(1-Methyl-1H-pyrazol-4-ylmethyl)-3'-(3-trifluoromethylphenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazine

https://huagongshe.com/reaction/220531

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylacetamideHCID 31374—
Reactant3-(Trifluoromethyl)phenylboronic acidHCID 2734388—
Reactant3'-Chloro-4-(1-methyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazineHCID 86641657—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
Product4-(1-Methyl-1H-pyrazol-4-ylmethyl)-3'-(3-trifluoromethylphenyl)-3,4,5,6-tetrahydro-2H-[1,2']bipyrazineHCID 5932179258%

Reaction Conditions

Temperature110 °C

Reaction Steps

Charge a carousel tube with 3-trifluoromethylbenzeneboronic acid (136 mg, 0.66 mmol), 3′-chloro-4-(1-methyl-1H-pyrazol-4-ylmethyl)-3,4,5,6-tetrahydro-2H-[1,2′]bipyrazinyl (160 mg, 0.55 mmol) and N,N-dimethylacetamide (1 mL). Add N,N-dimethylacetamide (3 mL) and potassium carbonate (185 mg, 1.32 mmol) and purge with nitrogen for about 45 min. Add water (2 mL, purged with nitrogen for 1 hr.) then tetrakis(triphenylphosphine)palladium(0) (0.003 g, 0.0025 mmol) and purge the reaction vessel for about 30 min. Heat at 110° C. overnight. Cool to room temperature, add water and extract with DCM (3×30 mL), and then concentrate the combined DCM extracts. Purify using silica gel chromatography, followed by reverse phase HPLC, to give the title compound (128 mg, 58%). MS (ES): m/z=403.1 [M+H]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08202873B2
Source datasetuspto-grants-2012_06
ORD IDord-9f282f01683641508d2828d474c33fda
Source noteuspto-grants-2012_06