Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378272Generated: October 30, 2026

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

https://huagongshe.com/reaction/378272

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrimethylamineHCID 1146—
ReactantMethylamine hydrochlorideHCID 6364545—
Reactant4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 10830093—
SolventEthanolHCID 702—
Product4-amino-N-(2-ethylamino-6-methylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 1071097254%

Reaction Steps

0.1 g (0.00031 mol) of 4-amino-N-(6-chloro-2-ethylamino-pyrimidin-4-yl)-benzenesulfonamide was dissolved in 20 ml of ethanol and stirred with 0.6 ml (0.0043 mol) of trimethylamine and 0.1 g (0.0015 mol) of methylamine hydrochloride 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 in 150 ml of 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 0.053 g (54%) of 4-amino-N-(2-ethylamino-6-methylamino-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p.: 261-263° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-2e4f447117ae4b1f96b12df214385e9c
Source noteuspto-grants-2000_02