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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405473Generated: November 2, 2026

Diisopropylethylamine → HCID 67041715, compound

https://huagongshe.com/reaction/1405473

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant1-(5-Trifluoromethyl-pyridin-2-yl)-piperazineHCID 667618—
ReactantMethyl 3-bromo-2-phenylquinoxaline-6-carboxylateHCID 86667202—
SolventDimethylformamideHCID 6228—
ProductHCID 67041715HCID 67041715—

Reaction Conditions

Temperature100 °C

Reaction Steps

Into a 8-mL sealed tube, was placed methyl 3-bromo-2-phenylquinoxaline-6-carboxylate (150 mg, 0.44 mmol, 1.00 equiv), 1-(5-(trifluoromethyl)pyridin-2-yl)piperazine (203.28 mg, 0.88 mmol, 2.00 equiv), DIEA (170.3 mg, 1.32 mmol, 3.00 equiv), N,N-dimethylformamide (3 mL). The resulting solution was stirred overnight at 100° C. in an oil bath. The reaction was then quenched by the addition of water. The resulting solution was extracted with 4×30 mL of dichloromethane and the organic layers combined and dried over anhydrous sodium sulfate. The solids were filtered out. The residue was applied onto a silica gel column with ethyl acetate/petroleum ether (1:50). This resulted in 210.8 mg (97%) of methyl 2-phenyl-3-(4-(5-(trifluoromethyl)pyridin-2-yl)piperazin-1-yl)quinoxaline-6-carboxylate as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916560B2
Source datasetuspto-grants-2014_12
ORD IDord-440bf1638f0049758b6e760d4c02e28d
Source noteuspto-grants-2014_12