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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378266Generated: October 30, 2026

Ethylamine → 4-amino-N-(6-ethylamino-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide

https://huagongshe.com/reaction/378266

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant4-amino-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 10852711—
SolventEthanolHCID 702—
Product4-amino-N-(6-ethylamino-2-methylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 1085327756%

Reaction Steps

0.314 g (0.001 mol) of 4-amino-N-(6-chloro-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide and 6.6 ml (0.1 mol) of ethylamine were stirred in 15 ml of ethanol in an autoclave at 130° C. for 3 hours. The reaction mixture was freed from solvent, the residue was suspended in 8 ml of ethanol and treated in an ultra-sound bath for 15 minutes. The precipitate was filtered off, dissolved in 10 ml of 0.1N NaOH and filtered. The filtrate was adjusted to pH 6 with 01N HCl. The precipitate was filtered off under suction, washed with water and dried. There was obtained 0.18 g (56%) of 4-amino-N-(6-ethylamino-2-methylamino-pyrimidin-4-yl)-benzenesulfonamide as white crystals; m.p.: 252° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-3d86680f96b441e0a962cb5deb85622f
Source noteuspto-grants-2000_02