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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1403643Generated: October 30, 2026

N-Methylisobutylamine → HCID 70664619, compound

https://huagongshe.com/reaction/1403643

Reaction equation

Participants

RoleNameHCIDCharge
ReactantN-MethylisobutylamineHCID 12249—
ReactantDiisopropylethylamineHCID 81531—
ReactantMethyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylateHCID 77231184—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 70664619HCID 7066461969%

Reaction Conditions

Temperature70 °C

Reaction Steps

To a solution of methyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylate (100 mg, 0.32 mmol) in DMSO (3 mL) was added DIEA (81.5 mg, 0.63 mmol) and isobutyl(methyl)amine (41 mg, 0.47 mmol), and the reaction was stirred overnight at 70° C. in an oil bath. The reaction mixture was cooled to room temperature, diluted with water (50 mL), and extracted with ethyl acetate (3×20 mL). The organic layers were combined, dried over magnesium sulfate, and concentrated in vacuo to give the residue, which was purified via silica gel column chromatography (1% ethyl acetate in petroleum ether) to afford methyl 2-(4-fluorophenyl)-3-(isobutyl(methyl)amino)quinoxaline-6-carboxylate as a light yellow solid (80 mg, 69%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08912188B2
Source datasetuspto-grants-2014_12
ORD IDord-9f50d460183b4d49ac4bf8185cd35fef
Source noteuspto-grants-2014_12