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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 879544Generated: October 25, 2026

Potassium Carbonate → 5-(5-bromo-2-methylpyridin-3-yl)-1-methyl-1H-indazole

https://huagongshe.com/reaction/879544

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
Reactant3,5-Dibromo-2-methylpyridineHCID 619705—
Reactant5-(Bromomethyl)-1-methyl-1H-indazoleHCID 49761704—
CatalystHCID 178418397HCID 178418397—
SolventWaterHCID 962—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
Product5-(5-bromo-2-methylpyridin-3-yl)-1-methyl-1H-indazoleHCID 86700366—
Product5-(5-bromo-6-methylpyridin-3-yl)-1-methyl-1H-indazoleHCID 86700367—

Reaction Conditions

Temperature105 °C

Reaction Steps

To a solution of 3,5-dibromo-2-methylpyridine (1.0 g, 3.99 mmol) and 5-(bromomethyl)-1-methyl-1H-indazole (772 mg, 4.38 mmol) in 1,4-dioxane (12 mL) was added Pd(PPh3)4 (231 mg, 0.20 mmol) and potassium carbonate solution (2 M aqueous, 6 mL, 12 mmol). The reaction mixture was stirred at 105° C. in a sealed tube for 1.5 h. The mixture was diluted with water (15 mL) and EtOAc (20 mL). The layers were separated, and the organic layer was dried, filtered, and concentrated in vacuo. The crude material was purified by CombiFlash (EtOAc w/5% MeOH and Hexanes) to give 5-(5-bromo-2-methylpyridin-3-yl)-1-methyl-1H-indazole and 5-(5-bromo-6-methylpyridin-3-yl)-1-methyl-1H-indazole.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08987250B2
Source datasetuspto-grants-2015_03
ORD IDord-ca3fabd5a2aa4e58945490cc7b3a090f
Source noteuspto-grants-2015_03