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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2106641Generated: October 29, 2026

3-Pyridinecarboxaldehyde → 4,5-Dihydro-6-methyl-4-((3-pyridinylmethylene)amino)-1,2,4-triazin-3(2H)-one

https://huagongshe.com/reaction/2106641

Reaction equation

Participants

RoleNameHCIDCharge
Reactant3-PyridinecarboxaldehydeHCID 10371—
Reactant4-Amino-6-methyl-2,5-dihydro-1,2,4-triazin-3-oneHCID 10975500—
CatalystHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
Product4,5-Dihydro-6-methyl-4-((3-pyridinylmethylene)amino)-1,2,4-triazin-3(2H)-oneHCID 86370—

Reaction Steps

26.8 g (0.25 mole) of pyridine-3-carbaldehyde and 1 drop of concentrated HCl are added at 60° C. to 32 g (0.25 mole) of 2,3,4,5-tetrahydro-3-oxo-4-amino-6-methyl-1,2,4-triazine dissolved in 250 ml of ethanol. After boiling for half an hour under reflux, the reaction mixture is cooled and the solid portion is isolated by filtration, washed with ether and dried to give the title compound of formula ##STR22## in the form of a colourless solid; m.p. 227°-228° C.; yield: 48 g (90%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04931439
Source datasetuspto-grants-1990_06
ORD IDord-051100895ca942cea5efa5ccfa6b894f
Source noteuspto-grants-1990_06