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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 378262Generated: October 29, 2026

Benzylamine → 4-amino-N-(2-amino-6-benzylamino-pyrimidin-4-yl)-benzenesulfonamide

https://huagongshe.com/reaction/378262

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
Reactant4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamideHCID 10732939—
SolventEthanolHCID 702—
Product4-amino-N-(2-amino-6-benzylamino-pyrimidin-4-yl)-benzenesulfonamideHCID 1201937541%

Reaction Conditions

Temperature130 °C

Reaction Steps

0.30 g (0.001 mol) of 4-amino-N-(2-amino-6-chloro-pyrimidin-4-yl)-benzenesulfonamide and 11 ml (0.1 mol) of benzylamine were dissolved in 15 ml of ethanol and stirred in an autoclave at 130° C. 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 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 0.15 g (41%) of 4-amino-N-(2-amino-6-benzylamino-pyrimidin-4-yl)-benzenesulfonamide as beige crystals; m.p.; 221° C. (dec.).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06030976
Source datasetuspto-grants-2000_02
ORD IDord-e55fdb86b89e4afbadb57b850da0ecda
Source noteuspto-grants-2000_02