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
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Benzoyl Peroxide | HCID 7187 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-bromobutanimide | HCID 67184 | — |
| Reactant | Methyl 2-cyano-3-fluoro-6-methylbenzoate | HCID 67192265 | — |
| Reactant | 1-(4,4-Difluorocyclohexyl)-piperidin-4-ylamine | HCID 67194236 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Solvent | Methyl pivalate | HCID 69027 | — |
| Solvent | Dichloromethane ethanol | HCID 21584144 | — |
| Product | 2-[1-(4,4-Difluorocyclohexyl)piperidin-4-yl]-5-fluoro-3-oxo-2,3-dihydro-1H-isoindole-4-carbonitrile | HCID 69674145 | 60.6% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08877944B2 |
|---|
| Source dataset | uspto-grants-2014_11 |
|---|
| ORD ID | ord-fe41265c19794c67b35eb10316e5112e |
|---|
| Source note | uspto-grants-2014_11 |
|---|