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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1388655Generated: November 2, 2026

2-Pyridone → 3-Bromo-1-methyl-5-(pyrimidin-4-yl)pyridin-2(1H)-one

https://huagongshe.com/reaction/1388655

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-PyridoneHCID 8871—
ReactantSodium MethoxideHCID 10942334—
Reactant3-Bromo-5-(pyrimidin-4-yl)pyridin-2(1H)-oneHCID 13276678—
SolventMethanolHCID 887—
SolventDimethylformamideHCID 6228—
Product3-Bromo-1-methyl-5-(pyrimidin-4-yl)pyridin-2(1H)-oneHCID 13645095—

Reaction Conditions

Temperature60 °C

Reaction Steps

20 g of 3-bromo-5-(4-pyrimidyl)-2(1H)-pyridone are suspended in 200 ml of dimethylformamide. A solution of 4.6 g of sodium methoxide in 300 ml of dry dimethylformamide and 15 ml of methanol is added to the pyridone suspension with stirring. The reaction mixture is filtered, 5.3 ml of methyl iodide are added to the filtrate and the mixture heated to 60° C. for 2 hours. After cooling to RT, the solution is concentrated in vacuo resulting in a liquid residue which crystallizes out upon addition of distilled H2O. The solid is stirred with 400 ml of distilled H2O, filtered, washed with H2O, isopropyl alcohol, and ether and dried, yielding 3-bromo-1-methyl-5-(4-pyrimidyl)-2-pyridone, M.P. 208°-210° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04432979
Source datasetuspto-grants-1984_02
ORD IDord-32d5059ab6e54c92a48805d8ffb0aa19
Source noteuspto-grants-1984_02