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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378287Generated: October 25, 2026

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

https://huagongshe.com/reaction/378287

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant4-chloro-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 19353555—
SolventEthanolHCID 702—
ProductN-(2,6-bis-methylamino-pyrimidin-4-yl)-4-chloro-benzenesulfonamideHCID 1777452845%

Reaction Conditions

Temperature140 °C

Reaction Steps

0.62 g (0.0019 mol) of 4-chloro-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 10 ml of ethanol, treated with 1.67 g (0.025 mol) of methylamine hydrochloride and 6.2 ml (0.044 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 filter cake was recrystallized in methanol/diethyl ether. There was obtained 0.28 g (45%) of N-(2,6-bis-methylamino-pyrimidin-4-yl)-4-chloro-benzenesulfonamide as white crystals; m.p. 272-273° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-b19d8bc201604946b3d9f6e15227402e
Source noteuspto-grants-2000_02