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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405591Generated: October 30, 2026

1-Butanol → Butyl 2-(4-fluorophenyl)-3-(piperidin-1-yl)quinoxaline-6-carboxylate

https://huagongshe.com/reaction/1405591

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1-ButanolHCID 263—
ReactantPiperidineHCID 8082—
ReactantMethyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylateHCID 77231184—
ProductButyl 2-(4-fluorophenyl)-3-(piperidin-1-yl)quinoxaline-6-carboxylateHCID 50991398—

Reaction Conditions

Temperature110 °C

Reaction Steps

Into a 10-mL sealed tube, was placed methyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylate (150 mg, 0.47 mmol, 1.00 equiv), piperidine (403 mg, 4.74 mmol, 10.00 equiv), butan-1-ol (2 mL). The resulting solution was stirred for overnight at 110° C. in an oil bath. The resulting mixture was concentrated under vacuum. This resulted in 150 mg (crude) of butyl 2-(4-fluorophenyl)-3-(piperidin-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-46ed332b8b67476989564d71aa0869fd
Source noteuspto-grants-2014_12