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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2283384Generated: October 31, 2026

Water → 7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxaline

https://huagongshe.com/reaction/2283384

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantSodium CarbonateHCID 10340—
Reactant1-Methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazoleHCID 2773987—
Reactant7-Bromo-2-chloroquinoxalineHCID 4913253—
CatalystHCID 178418397HCID 178418397—
Solvent1,2-DimethoxyethaneHCID 8071—
Product7-bromo-2-(1-methyl-1H-pyrazol-4-yl)quinoxalineHCID 5784325882.1%

Reaction Steps

Under N2, 7-bromo-2-chloro-quinoxaline (20 g; 82.1 mmol), 1-methyl-4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)-1H-pyrazole (17.1 g; 82.1 mmol), 2M sodium carbonate aqueous solution (41.1 mL; 82.1 mmol) in ethylene glycol dimethyl ether (200 mL) were degassed by bubbling nitrogen through for 15 minutes. Tetrakis(triphenylphosphine)palladium (0) (0.95 g; 0.82 mmol) was added and heated at reflux for 15 hours. The reaction mixture was poured into water and extracted with EtOAc. The organic layer was dried over MgSO4, filtered and evaporated to dryness to give 29.9 g. The crude compound was purified by chromatography over silica gel (Irregular SiOH, 20-45 μm, 1000 g MATREX; mobile phase 0.1% NH4OH, 98% DCM, 2% CH3OH). The pure fractions were collected and concentrated till dryness to give 19.5 g (82%) of 7-Bromo-2-(1-methyl-1H-pyrazol-4-yl)-quinoxaline. MP=172° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09145394B2
Source datasetuspto-grants-2015_09
ORD IDord-679c04606d9340d897799cb949f03c05
Source noteuspto-grants-2015_09