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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2395615Generated: October 31, 2026

Imidazole → 4-(1H-imidazol-1-yl)-N-methyl-6-(morpholin-4-yl)-N-phenyl-1,3,5-triazin-2-amine

https://huagongshe.com/reaction/2395615

Reaction equation

Participants

RoleNameHCIDCharge
ReactantImidazoleHCID 795—
ReactantSodium HydroxideHCID 14798—
Reactant2-chloro-4-(N-methyl-N-phenylamino)-6-morpholino-1,3,5-triazineHCID 10828440—
SolventDimethylformamideHCID 6228—
Product4-(1H-imidazol-1-yl)-N-methyl-6-(morpholin-4-yl)-N-phenyl-1,3,5-triazin-2-amineHCID 66770752.8%

Reaction Steps

The obtained 2-chloro-4-(N-methyl-N-phenylamino)-6-morpholino-1,3,5-triazine (135 mg, 0.457 mmol) was dissolved in DMF (5 ml), added with sodium hydroxide (19.2 mg, 0.480 mmol) and imidazole (32.7 mg, 0.480 mmol) and stirred at 110° C.-120° C. for 5 hours. After allowing to cool to room temperature, the solvent was removed under reduced pressure. The residue was added with ethyl acetate and water, and then shaken for mixing. The organic layer was separated from the mixture, washed with water and dried over anhydrous magnesium sulfate. The solvent was removed under reduced pressure and the residue was purified by silica gel column chromatography, using dichloromethane and methanol (20:1) as eluant, to obtain 71.3 mg (yield: 52.8%) of the titled compound as colorless crystals.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05489591
Source datasetuspto-grants-1996_02
ORD IDord-c67816be3c4f4b609c8a3f134d14aed4
Source noteuspto-grants-1996_02