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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1617012Generated: November 1, 2026

Pyridine → 2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamide

https://huagongshe.com/reaction/1617012

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantMethanesulfonyl chlorideHCID 31297—
Reactant2,5-Diamino-benzenesulfonamide methanesulfonateHCID 25164641—
SolventAcetonitrileHCID 6342—
Product2-Amino-5-[(methylsulfonyl)amino]benzenesulfonamideHCID 2495065786.3%

Reaction Conditions

Temperature23 °C

Reaction Steps

2,5-Diamino-benzenesulfonamide methanesulfonate (1.80 kg, 6.35 mol) was suspended in acetonitrile (24 L). Pyridine (1.55 L, 19.1 mol) was added, followed by the careful slow addition of methanesulfonyl chloride (517 mL, 6.68 mol). After stirring at 23° C. for 20 h, the mixture was partially concentrated in vacuo at 55° C. Water (18 L) was added to the concentrate, and the resulting suspension was stirred at 23° C. for 2 h. The solid was filtered and was then washed with water (4 L) and air dried on the filter. The solid was suspended in absolute ethanol (9 L), stirred at 23° C. for 9 h, and was then filtered. The solid was washed with absolute ethanol (2×2 L), and was then further dried in vacuo at 50° C. to afford the desired product, 2-amino-5-methanesulfonylamino-benzenesulfonamide (1.45 kg, 5.48 mol, 86%), as a purple solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08765741B2
Source datasetuspto-grants-2014_07
ORD IDord-0068ea6b773946dc90dc9d70d24c6fd6
Source noteuspto-grants-2014_07