Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 927314Generated: November 1, 2026

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

https://huagongshe.com/reaction/927314

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 numberUS09290478B2
Source datasetuspto-grants-2016_03
ORD IDord-4b91a020adac45cfbb8f9bd48f171b67
Source noteuspto-grants-2016_03