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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1294425Generated: October 30, 2026

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

https://huagongshe.com/reaction/1294425

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 (comp. 20).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07241458B1
Source datasetuspto-grants-2007_07
ORD IDord-4e7220904d584d85929dd2954c154e1a
Source noteuspto-grants-2007_07