Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2223824Generated: November 4, 2026

Water → N,N'-diphenyl-N''-(4-pyridylmethyl)-1,3,5-triazine-2,4,6-triamine

https://huagongshe.com/reaction/2223824

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant1,3,5-Triazine-2,4-diamine, 6-chloro-N2,N4-diphenyl-HCID 16088—
Reactant4-PyridinemethanamineHCID 77317—
ReactantDiisopropylethylamineHCID 81531—
SolventAcetonitrileHCID 6342—
ProductN,N'-diphenyl-N''-(4-pyridylmethyl)-1,3,5-triazine-2,4,6-triamineHCID 10150345—

Reaction Conditions

Temperature80 °C

Reaction Steps

A 200 mg portion of 6-chloro-N,N′-diphenyl-1,3,5-triazine-2,4-diamine was dissolved in 10.0 ml of acetonitrile, and 145 mg of 4-(aminomethyl)pyridine and 0.585 ml of diisopropylethylamine were added thereto and stirred overnight at 80° C. The reaction solution was cooled down to room temperature, and then mixed with water and extracted with chloroform. The organic layer was washed with 5% citric acid and saturated brine and then dried using anhydrous magnesium sulfate. The solvent was evaporated under a reduced pressure, the thus obtained residue was applied to a silica gel column chromatography and eluted with ethyl acetate:n-hexane (2:1), and then the thus obtained crude product was crystallized from ethyl acetate/n-hexane, thereby obtaining 107 mg of N,N′-diphenyl-N″-(4-pyridylmethyl)-1,3,5-triazine-2,4,6-triamine as light red crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07375222B2
Source datasetuspto-grants-2008_05
ORD IDord-0567f529f8734978bf303f29f1f859c5
Source noteuspto-grants-2008_05