Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 716897Generated: October 30, 2026

Diisopropylethylamine → Methyl 3-(4-(4-methoxyphenyl)piperidin-1-yl)-2-phenylquinoxaline-6-carboxylate

https://huagongshe.com/reaction/716897

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiisopropylethylamineHCID 81531—
Reactant4-(4-Methoxyphenyl)piperidineHCID 10679270—
ReactantMethyl 3-chloro-2-phenylquinoxaline-6-carboxylateHCID 77231183—
SolventDimethylformamideHCID 6228—
ProductMethyl 3-(4-(4-methoxyphenyl)piperidin-1-yl)-2-phenylquinoxaline-6-carboxylateHCID 6704198979.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of methyl 3-chloro-2-phenylquinoxaline-6-carboxylate (150 mg, 0.50 mmol, 1.00 equiv), 4-(4-methoxyphenyl)piperidine (191 mg, 1.00 mmol, 2.00 equiv), and DIEA (194.8 mg, 1.51 mmol, 5.00 equiv) in DMF (4 mL) was placed in an 8-mL sealed tube and stirred overnight at 100° C. in an oil bath. The reaction was then quenched by the addition of water, and the resulting mixture was concentrated under vacuum. Purification via silica gel column (ethyl acetate/petroleum ether (1:50)) yielded 179.6 mg (63%) of methyl 3-(4-(4-methoxyphenyl)piperidin-1-yl)-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-26d8f612214a4077857539352d288cba
Source noteuspto-grants-2015_11