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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1363890Generated: October 30, 2026

Sodium Hydroxide → HCID 486392, compound

https://huagongshe.com/reaction/1363890

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 (comp. 52).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07887845B2
Source datasetuspto-grants-2011_02
ORD IDord-a5a67f10f5fa421c9cd9909b134bc90a
Source noteuspto-grants-2011_02