Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610817Generated: November 2, 2026

Triethylamine → N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-tert-butyl-benzenesulfonamide

https://huagongshe.com/reaction/610817

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant4-tert-butyl-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 19353535—
SolventEthanolHCID 702—
ProductN-(2,6-bis-methylamino-pyrimidin-4-yl)-4-tert-butyl-benzenesulfonamideHCID 1777452533%

Reaction Conditions

Temperature140 °C

Reaction Steps

0.47 g (0.0013 mol) of 4-tert-butyl-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 10 ml of ethanol, treated with 1.3 g (0.019 mol) of methylamine hydrochloride and 4.7 ml (0.034 mol) of triethylamine and stirred in an autoclave at 140° C. for 18 hours. The mixture was freed completely from solvent, the residue was partitioned in ethyl acetate/water and the insoluble constituents were filtered off under suction. The filtered cake was recrystallized in methanol/diethyl ether. There was obtained 0.15 g (33%) of N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-tert-butyl-benzenesulfonamide as white crystals; m.p. 316-318° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998665
Source datasetuspto-grants-1999_12
ORD IDord-f9442ef4688447fa8f64b455bb233abb
Source noteuspto-grants-1999_12