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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716951Generated: October 30, 2026

2-Phenylethylamine hydrochloride → Methyl 3-(phenethylamino)-2-phenylquinoxaline-6-carboxylate

https://huagongshe.com/reaction/716951

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-Phenylethylamine hydrochlorideHCID 9075—
ReactantPotassium CarbonateHCID 11430—
ReactantMethyl 3-bromo-2-phenylquinoxaline-6-carboxylateHCID 86667202—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(phenethylamino)-2-phenylquinoxaline-6-carboxylateHCID 67041739—

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 10-mL sealed tube, was placed methyl 3-bromo-2-phenylquinoxaline-6-carboxylate (150 mg, 0.44 mmol, 1.00 equiv), 2-phenylethanamine hydrochloride (207.8 mg, 1.32 mmol, 3.00 equiv), potassium carbonate (304.4 mg, 2.21 mmol, 5.00 equiv), N,N-dimethylformamide (2 mL). The resulting solution was stirred overnight at 100° C. in an oil bath. The reaction was then quenched by the addition of 20 mL of water. The resulting solution was extracted with 3×50 mL of ethyl acetate and the organic layers combined. The organic layer was dried over anhydrous sodium sulfate and concentrated under vacuum. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:50). This resulted in 120 mg (71%) of methyl 3-(phenethylamino)-2-phenylquinoxaline-6-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09193693B2
Source datasetuspto-grants-2015_11
ORD IDord-dffb684073444297a31346e7c41c2e7d
Source noteuspto-grants-2015_11