Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1431437Generated: November 2, 2026

2-Pyrrolidone → 1-(4-Bromo-5,7-difluoro-3-methylquinolin-2-yl)pyrrolidin-2-one

https://huagongshe.com/reaction/1431437

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyrrolidoneHCID 12025—
ReactantPotassium Phosphate, TribasicHCID 62657—
Reactant(1S,2S)-(+)-N,N'-Dimethylcyclohexane-1,2-diamineHCID 13822957—
Reactant2,4-Dibromo-5,7-difluoro-3-methylquinolineHCID 59631114—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
Solvent1,4-DioxaneHCID 31275—
Product1-(4-Bromo-5,7-difluoro-3-methylquinolin-2-yl)pyrrolidin-2-oneHCID 59631073—

Reaction Conditions

Temperature110 °C

Reaction Steps

The 2,4-dibromo-5,7-difluoro-3-methylquinoline (500 mg, 1.50 mmol), pyrrolidin-2-one (0.110 mL, 1.50 mmol), copper (I) iodide (14 mg, 0.074 mmol), (1S,2S)—N1,N2-dimethylcyclohexane-1,2-diamine (0.023 mL, 0.150 mmol) and potassium phosphate tribasic (630 mg, 3.00 mmol) were slurried in dioxane (5 mL) and stirred in a microwave reactor at 110° C. for 2 h. The resulting slurry was dissolved and partitioned between water and EtOAc (2×75 mL). The combined organic layers were washed with brine (1×50 mL) and dried over magnesium sulfate. The crude product was purified by medium pressure chromatography (silica, 0 to 100% EtOAc:DCM) to give 1-(4-bromo-5,7-difluoro-3-methylquinolin-2-yl)pyrrolidin-2-one. Mass Spectrum (ESI) m/e=341.0 (M+1).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08940724B2
Source datasetuspto-grants-2015_01
ORD IDord-3920e3decf2842c28c1a5c1794b92733
Source noteuspto-grants-2015_01