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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1966677Generated: October 30, 2026

Potassium Carbonate → 5-{1-tert-Butyl-2-[2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-1H-benzimidazol-5-yl}-pyrimidin-2-ylamine

https://huagongshe.com/reaction/1966677

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant5-[2-(2-bromo-phenyl)-1-tert-butyl-1H-benzimidazol-5-yl]-pyrimidin-2-ylamineHCID 58541953—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventDimethylformamideHCID 6228—
Product5-{1-tert-Butyl-2-[2-(1-methyl-1H-pyrazol-4-yl)-phenyl]-1H-benzimidazol-5-yl}-pyrimidin-2-ylamineHCID 5854197034%

Reaction Conditions

Temperature120 °C

Reaction Steps

To a solution of 5-[2-(2-bromo-phenyl)-1-tert-butyl-1H-benzimidazol-5-yl]-pyrimidin-2-ylamine (70 mg, 0.17 mmol) in DMF (5 mL) and H2O (1 mL) are added 1-methylpyrazole-4-boronic acid pinacol ester (52 mg, 0.25 mmol), Pd(PPh3)4 (19 mg, 0.017 mmol) and K2CO3 (23 mg, 0.17 mmol) at room temperature. The solution is heated to 120° C. for 1 hour in a microwave reactor. The solution is cooled down and 3-mercaptopropyl-functionalized silica gel (500 mg) is added. The solution is stirred for 15 minutes and then filtered. The filtrate is washed with H2O (10 mL) and is extracted with EtOAc (3×15 mL). The combined organic layer is dried (MgSO4), filtered and concentrated. The residue is purified by silica gel flash chromatography eluting with 10% MeOH in CH2Cl2 to afford the title compound (24 mg, 34%) as a white solid. LCMS (ESMS): m/z 424.20 (M++1)

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08420655B2
Source datasetuspto-grants-2013_04
ORD IDord-4808f7d8cc244fb1a7d3175ad589f0aa
Source noteuspto-grants-2013_04