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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378261Generated: October 29, 2026

Ethylamine → 4-Amino-N-(2-amino-6-ethylamino-pyrimidin-4-yl)-benzenesufonamide

https://huagongshe.com/reaction/378261

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthylamineHCID 6341—
Reactant4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamideHCID 10732939—
SolventEthanolHCID 702—
Product4-Amino-N-(2-amino-6-ethylamino-pyrimidin-4-yl)-benzenesufonamideHCID 1073359853%

Reaction Conditions

Temperature130 °C

Reaction Steps

0.50 g (0.00167 mol) of 4-amino-N-(2-amino-6-chloropyrimidin-4-yl)-benzenesufonamide and 11 ml (0.167 mol) of ethylamine were dissolved in 20 ml of ethanol and stirred in an autoclave at 130° C. for 4 hours. The reaction mixture was freed from solvent, the residue was suspended in 5 ml of ethanol and treated in an ultrasound bath for 15 minutes. The precipitate was filtered off, dissolved 10 ml of 0.1N NaOH and filtered. The filtrate was adjusted to pH 6 with 0.1N HCl. The precipitate was filtered off under suction, washed with water and dried. There was obtained 0.271 g (53%) of 4-amino-N-(2-amino-6-ethylamino-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p. 272-274° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-0edc4226fa484de9b7f2dc1416f466e8
Source noteuspto-grants-2000_02