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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 589555Generated: October 31, 2026

p-Toluenesulfonic acid → 4-(4-Methoxypyrimidin-2-ylamino)benzonitrile

https://huagongshe.com/reaction/589555

Reaction equation

Participants

RoleNameHCIDCharge
Reactantp-Toluenesulfonic acidHCID 6101—
Reactant4-AminobenzonitrileHCID 13396—
ReactantSodium BicarbonateHCID 516892—
Reactant2-Chloro-4-methoxypyrimidineHCID 588935—
SolventIsopropanolHCID 3776—
Solvent1,4-DioxaneHCID 31275—
Product4-(4-Methoxypyrimidin-2-ylamino)benzonitrileHCID 5227069655.3%

Reaction Conditions

Temperature105 °C

Reaction Steps

1,4-Dioxane (100 ml) was added to a mixture of 2-chloro-4-methoxypyrimidine (20 gm), 4-aminobenzonitrile (16.33 gm) and p-toluene sulfonic acid (42.12 gm). The mixture was then heated to 100 to 110° C. and stirred for 14 hours. The solution was then cooled to room temperature and basified with saturated sodium bicarbonate solution. The layers were separated and the aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with water and then concentrated to obtain a residual solid. The residual solid obtained was slurried in isopropyl alcohol at room temperature for 30 minutes and filtered. The solid obtained was then dried to give 17.3 gm of 4-(4-methoxypyrimidin-2-ylamino)benzonitrile.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09233935B2
Source datasetuspto-grants-2016_01
ORD IDord-52710eacc47947b9b3c1beeca4257525
Source noteuspto-grants-2016_01