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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1048969Generated: October 26, 2026

Sodium Carbonate → HCID 178506243, compound

https://huagongshe.com/reaction/1048969

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium CarbonateHCID 10340—
Reactant6-bromo-1-cyclopropyl-2-(5-trifluoromethyl-pyridin-3-yl)-1H-benzoimidazoleHCID 66692676—
ReactantHCID 178431094HCID 178431094—
CatalystHCID 178418397HCID 178418397—
SolventEthanol toluene waterHCID 86587398—
ProductHCID 178506243HCID 178506243—

Reaction Conditions

Temperature80 °C

Reaction Steps

To a solution of 6-bromo-1-cyclopropyl-2-(5-trifluoromethyl-pyridin-3-yl)-1H-benzoimidazole (0.15 g, 0.00026 mol) in ethanol toluene water (6 ml 3 ml 1.5 ml respectively) mixture in a sealed tube was added 3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-1H-pyrazole (0.1 g, 0.00052 mol) and Na2CO3 (0.082 g, 0.000785 mol) and argon was purged for 15 min. Then Pd (PPh3)4 (0.015 g, 0.000013 mol) was added and heated at 80° C. for 5 h. The solvent was evaporated and the resulting residue was added water. The aqueous layer was extracted with ethyl acetate (3×20 ml). The combined organic layers were washed with brine dried over Na2SO4 and concentrated under vacuum to afford the crude compound which was purified by column chromatography to obtain title compound 1-cyclopropyl-6-(1H-pyrazol-3-yl)-2-[5-(trifluoromethyl)pyridin-3-yl]-1H-benzimidazole (321) as an off white solid. NMR (400 MHz, DMSO-d6), δ: 12.85 (s, 1H), 9.49 (s, 1H), 9.12 (s, 1H), 8.75 (s, 1H), 8.09 (s, 1H), 7.79-7.67 (m, 3H), 7.54-7.52 (m, 1H), 6.79 (s, 1H), 3.96 (bs, 1H), 1.15 (d, J=5.6 Hz, 2H), 0.73 (bs, 2H). MS (M+1): 370.6, Purity 99.94%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09382226B2
Source datasetuspto-grants-2016_07
ORD IDord-6c5331d22ef9473c8d6d52559d86c631
Source noteuspto-grants-2016_07