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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1405295Generated: November 1, 2026

(2R)-2-(Trifluoromethyl)pyrrolidine → (R)-methyl 2-(4-fluorophenyl)-3-(2-(trifluoromethyl)pyrrolidin-1-yl)quinoxaline-6-carboxylate

https://huagongshe.com/reaction/1405295

Reaction equation

Participants

RoleNameHCIDCharge
Reactant(2R)-2-(Trifluoromethyl)pyrrolidineHCID 7015082—
ReactantMethyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylateHCID 77231184—
SolventDimethyl SulfoxideHCID 679—
Product(R)-methyl 2-(4-fluorophenyl)-3-(2-(trifluoromethyl)pyrrolidin-1-yl)quinoxaline-6-carboxylateHCID 70654237—

Reaction Conditions

Temperature130 °C

Reaction Steps

To a solution of methyl 3-chloro-2-(4-fluorophenyl)quinoxaline-6-carboxylate (270 mg, 0.85 mmol) in DMSO (1 mL) was added (R)-2-(trifluoromethyl)pyrrolidine (275 mg, 1.99 mmol). The resulting solution was stirred 7 days at 130° C. and then evaporated in vacuo. The residue was diluted with petroleum ether (15 mL) and filtered. The filtrate was concentrated and purified by a silica gel column chromatography with 2%-10% ethyl acetate in petroleum ether to afford (R)-methyl 2-(4-fluorophenyl)-3-(2-(trifluoromethyl)pyrrolidin-1-yl)quinoxaline-6-carboxylate as a yellow solid (35 mg, crude).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08916561B2
Source datasetuspto-grants-2014_12
ORD IDord-7d9db9235cc0473298fe6487a8ca74a4
Source noteuspto-grants-2014_12