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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1910855Generated: November 2, 2026

Water → 3-{1-[6-(5-Bromopyrimidin-2-yl)pyridin-2-ylmethyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile

https://huagongshe.com/reaction/1910855

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantCesium carbonateHCID 10796—
Reactant3-(6-Oxo-1,6-dihydropyridazin-3-yl)benzonitrileHCID 20326520—
Reactant5-Bromo-2-(6-bromomethylpyridin-2-yl)-pyrimidineHCID 58138080—
SolventDimethylformamideHCID 6228—
Product3-{1-[6-(5-Bromopyrimidin-2-yl)pyridin-2-ylmethyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrileHCID 66922953—

Reaction Conditions

Temperature80 °C

Reaction Steps

2.3 54.6 mg (0.166 mmol) of 5-bromo-2-(6-bromomethylpyridin-2-yl)-pyrimidine and 54.1 mg (0.166 mmol) of caesium carbonate are added to a suspension of 32.7 mg (0.166 mmol) of 3-(6-oxo-1,6-dihydropyridazin-3-yl)benzonitrile in 0.5 ml of DMF, and the mixture is stirred for 18 hours at 80° C. The reaction mixture is added to water. The precipitate formed is filtered off with suction, washed with water and dried in vacuo, giving 3-{1-[6-(5-bromopyrimidin-2-yl)pyridin-2-ylmethyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile as slightly brownish crystals; ESI 445, 447;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08604036B2
Source datasetuspto-grants-2013_12
ORD IDord-67c8d1d186e04c7aadfc194d1522e68f
Source noteuspto-grants-2013_12