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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1070950Generated: October 29, 2026

Sodium Hydroxide → HCID 486392, compound

https://huagongshe.com/reaction/1070950

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium HydroxideHCID 14798—
ReactantDiisopropylethylamineHCID 81531—
Reactant4-amino-3,5-dimethylbenzonitrileHCID 278944—
ReactantHCID 86583607HCID 86583607—
SolventDichloromethaneHCID 6344—
SolventN-methyl-2-pyrrolidoneHCID 13387—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 486392HCID 486392202.3%

Reaction Conditions

Temperature195 °C

Reaction Steps

4-[[4-[(4-chloro-5-methyl-2-pyrimidinyl]amino]benzonitrile (0.01541 mol), 4-amino-3,5-dimethyl-benzonitrile (0.00219 mol), 1-methyl-2-pyrrolidinone (4 ml), 1,4-dioxane (15 ml) and diisopropylethylamine (0.0154 mol) were combined in a flask under a stream of argon and heated at 160-230° C. for 16 hours. CH2Cl2 and 1N NaOH were added, and the mixture was stirred 1 hour and filtered to give a brown solid (*). The CH2Cl2 filtrate was separated and was evaporated and purified by flash column chromatography (eluent: 2% CH3OH/CH2Cl2). The desired fractions were combined, evaporated and the residue was stirred in CH2Cl2. The solid precipitate was filtered off, combined with the brown solid (*) and recrystallized from CH3CN. The precipitate was filtered off and dried, yielding 1.57 g (29%) of 4-[[2-[(4-cyanophenyl)amino]-5-methyl-4-pyrimidinyl]amino]-3,5-dimethylbenzonitrile (compound 89).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06903213B2
Source datasetuspto-grants-2005_06
ORD IDord-813d367786df433c8f44798775937947
Source noteuspto-grants-2005_06