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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070952Generated: October 31, 2026

Water → 4-[[4-(2,4,6-Trimethylphenoxy)-2-pyrimidinyl]amino]benzonitrile

https://huagongshe.com/reaction/1070952

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
Reactant2,4,6-TrimethylphenolHCID 10698—
ReactantSodium hydrideHCID 24758—
Reactant4-((4-Chloropyrimidin-2-yl)amino)benzonitrileHCID 11195595—
Solvent1,4-DioxaneHCID 31275—
Product4-[[4-(2,4,6-Trimethylphenoxy)-2-pyrimidinyl]amino]benzonitrileHCID 48876789.4%

Reaction Steps

To a suspension of NaH (0.006 mol) in 1,4-dioxane (30 ml), 2,4,6-trimethyl-phenol (0.006 mol) was added. The mixture was stirred for 15 minutes at room temperature, and a clear solution formed, 4-[(4-chloro-2-pyrimidinyl)amino]benzonitrile (0.004 mol) was added, and the reaction mixture was heated to reflux under Argon for 15 hours. The reaction mixture was allowed to cool to room temperature, 0.5 ml of water was added, followed by 4 g of silica gel, and the solvent was evaporated. The residue was purified by flash column chromatography over silica gel (eluent gradient: CH2Cl2:CH3OH 100:0:0 to 97:3). The pure fractions were collected and the solvent was evaporated, yielding 1.18 g (89.4%) of 4-[[4-(2,4,6-trimethylphenoxy)-2-pyrimidinyl]amino]benzonitrile (compound 58).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903213B2
Source datasetuspto-grants-2005_06
ORD IDord-9addd6b18e964542893aed354d1b3127
Source noteuspto-grants-2005_06