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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 610836Generated: November 1, 2026

HCID 10689660, compound → HCID 19353518, compound

https://huagongshe.com/reaction/610836

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 10689660HCID 10689660—
ReactantHCID 178418361HCID 178418361—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
ProductHCID 19353518HCID 1935351857%

Reaction Steps

0.5 g (0.0014 mol) of 4-amino-N-(2-bromo-6-methylamino-pyridin-4-yl)-benzenesulfonamide was dissolved in 25 ml of ethanol, treated with 0.05 g of Pd/C and hydrogenated with hydrogen gas under normal pressure for 1 hour. The catalyst was filtered off, the filtrate was concentrated and the residue was dissolved in 10 ml of 1N NaOH, filtered and the filtrate was then adjusted pH 8 by means of 1N HCl. The precipitate which separated slowly was filtered off under suction, rinsed and dried in a high vacuum. There was obtained 0.22 g (57%) of 4-amino-N-(2-methylamino-pyridin-4-yl)-benzenesulfonamide as white crystals; m.p.: >261° C. (dec).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05998665
Source datasetuspto-grants-1999_12
ORD IDord-c1f66338617f48ae8b5611d2d4295fa5
Source noteuspto-grants-1999_12