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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1620792Generated: October 31, 2026

Isopropanol → 3-Bromo-1-phenyl-5-(pyridin-2-yl)-1,2-dihydropyridin-2-one

https://huagongshe.com/reaction/1620792

Reaction equation

Participants

RoleNameHCIDCharge
ReactantIsopropanolHCID 3776—
ReactantDimethylformamideHCID 6228—
ReactantN-bromobutanimideHCID 67184—
Reactant1-Phenyl-5-pyridin-2-ylpyridin-2-oneHCID 20872595—
SolventWaterHCID 962—
Product3-Bromo-1-phenyl-5-(pyridin-2-yl)-1,2-dihydropyridin-2-oneHCID 2231906586.4%

Reaction Conditions

Temperature30 °C

Reaction Steps

5-(2-Pyridyl)-1-phenyl-1,2-dihydropyridine-2-one (300 g), N-bromosuccinimide (236.5 g) and N,N-dimethylformamide (1.8 L) were placed in a 10-L reactor, and the reaction mixture was stirred at 30° C. (external temperature) in a nitrogen stream for 3 hours and 15 minutes. 2-Propanol (4.2 L) was added dropwise to the reaction mixture over a period of 9 minutes, followed by adding thereto water (2.1 L) over a period of 7 minutes. The resulting mixture was heated at 85° C. (external temperature) with stirring. After confirming the dissolution of the contents, the resulting solution was stirred at an external temperature of 55° C. for 1 hour. Thereafter, the solution was stirred at 40° C. (external temperature) for another 22 minutes, at 30° C. (external temperature) for further another 23 minutes, and then at 10° C. (external temperature) for still another 15 hours and 15 minutes. The reaction mixture was filtered and the precipitate was washed with 50% 2-propanol-water (2.4 L) and then dried under reduced pressure (60° C., 6 hours) to obtain 341.45 g of 3-bromo-5-(2-pyridyl)-1-phenyl-1,2-dihydropyridine-2-one. Yield: 86.4%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08772497B2
Source datasetuspto-grants-2014_07
ORD IDord-2f2ff32c269c49f49b2e93ca0ff9dfde
Source noteuspto-grants-2014_07