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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 912611Generated: November 2, 2026

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

https://huagongshe.com/reaction/912611

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 numberUS08026248B2
Source datasetuspto-grants-2011_09
ORD IDord-ea80204369fe4fc0aa533ccefaf92032
Source noteuspto-grants-2011_09