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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 41367Generated: October 28, 2026

Hydrochloric Acid → 4-((4-Amino-5,6-dichloropyrimidin-2-yl)amino)benzonitrile

https://huagongshe.com/reaction/41367

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
ReactantN-methyl-2-pyrrolidoneHCID 13387—
Reactant4-AminobenzonitrileHCID 13396—
Reactant2,5,6-Trichloropyrimidin-4-amineHCID 15850196—
SolventDiethyl EtherHCID 3283—
Solvent1,4-DioxaneHCID 31275—
Product4-((4-Amino-5,6-dichloropyrimidin-2-yl)amino)benzonitrileHCID 221700986.8%

Reaction Conditions

Temperature145 °C

Reaction Steps

To a flask under Argon was added 4-amino-2,5,6-trichloropyrimidine (0.08564 mol), 4-amino-benzonitrile (0.1071 mol), 1-methyl-2-pyrrolidinone (17 ml) and HCl in diethylether (1M; 85.6 ml). The mixture was placed in an oil bath at 130° C. under a stream of nitrogen until the ether was gone. An additional 10 ml of 1-methyl-2-pyrrolidinone was added. The mixture was heated at 145° C. for 16 hours under argon. 1,4-Dioxane was added. The mixture was refluxed, cooled, then filtered. The filtrate was evaporated. The residue was dissolved in CH2Cl2, washed with 1 N NaOH, then filtered. The solid was dissolved in 2-propanone, evaporated onto silica gel, and chromatographed using 1-3% 2-propanone in hexane as eluent. The pure fractions were collected and the solvent was evaporated, yielding 1.63 g (6.8%) of 4-[(4-amino-5,6-dichloro-2-pyrimidinyl)amino]benzonitrile (interm. 12).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08530655B2
Source datasetuspto-grants-2013_09
ORD IDord-52d15fc4d6fc4139af8d6f37a462d641
Source noteuspto-grants-2013_09