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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1408392Generated: October 25, 2026

Triphenylphosphine → 3-{1-[3-(5-Methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile

https://huagongshe.com/reaction/1408392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriphenylphosphineHCID 11776—
Reactant3-(6-Oxo-1,6-dihydropyridazin-3-yl)benzonitrileHCID 20326520—
ReactantDiisopropyl diazodicarboxylateHCID 22145704—
Reactant[3-(5-Methylpyrimidin-2-yl)phenyl]methanolHCID 59484945—
SolventTetrahydrofuranHCID 8028—
Product3-{1-[3-(5-Methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrileHCID 59484891—

Reaction Steps

8.3 147 μl (0.75 mmol) of diisopropyl diazodicarboxylate are added dropwise to a suspension of 98.6 mg (0.50 mmol) of 3-(6-oxo-1,6-dihydropyridazin-3-yl)benzonitrile, 100 mg (0.50 mmol) of [3-(5-methylpyrimidin-2-yl)phenyl]methanol and 197 mg (0.75 mmol) of triphenylphosphine in 3 ml of THF, and the resultant solution is stirred at room temperature for 18 hours. The reaction mixture is evaporated in vacuo, and 2-propanol is added to the residue. The resultant precipitate is filtered off with suction and chromatographed on a silica gel column with dichloromethane/methanol as eluent: 3-{1-[3-(5-methylpyrimidin-2-yl)benzyl]-6-oxo-1,6-dihydropyridazin-3-yl}benzonitrile (“A15”) as yellowish solid; ESI 380;

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08921357B2
Source datasetuspto-grants-2014_12
ORD IDord-0258cf21d3de434b872b5784d05811f8
Source noteuspto-grants-2014_12