Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 333221Generated: October 30, 2026

Benzoyl Peroxide → 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-5-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carbonitrile

https://huagongshe.com/reaction/333221

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzoyl PeroxideHCID 7187—
ReactantTriethylamineHCID 8471—
ReactantN-bromobutanimideHCID 67184—
ReactantMethyl 2-cyano-3-fluoro-6-methylbenzoateHCID 67192265—
Reactant1-(4,4-Difluorocyclohexyl)-piperidin-4-ylamineHCID 67194236—
SolventDichloromethaneHCID 6344—
SolventMethyl pivalateHCID 69027—
SolventDichloromethane ethanolHCID 21584144—
Product2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-5-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carbonitrileHCID 6967414560.6%

Reaction Conditions

Temperature85 °C

Reaction Steps

To a solution of methyl 2-cyano-3-fluoro-6-methylbenzoate (208 mg, 1.07 mmol) in methyl pivalate (2 mL), N-bromosuccinimide (310 mg, 1.74 mmol) and benzoylperoxide (20 mg, 0.097 mmol) were added. The reaction mixture was stirred at 85° C. under nitrogen atmosphere for 3 hours. Crude was filtered on Gooch and washed with toluene. Volatiles were evaporated and the residue was dissolved in acetonitrile (3 mL). Triethylamine (0.41 mL, 2.9 mmol) and 1-(4,4-difluorocyclohexyl)-piperidin-4-ylamine (280 mg, 0.97 mmol) were added and the reaction mixture was stirred at 90° C. for 3 hours. Crude was diluted with dichloromethane and washed with 15% ammonium hydroxide Organic phase was dried over sodium sulfate, filtered and evaporated. Column chromatography (dichloromethane/ethanol:95/5) afforded title compound (222 mg, 60% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08877944B2
Source datasetuspto-grants-2014_11
ORD IDord-fe41265c19794c67b35eb10316e5112e
Source noteuspto-grants-2014_11