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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1751207Generated: October 28, 2026

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

https://huagongshe.com/reaction/1751207

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 numberUS09156832B2
Source datasetuspto-grants-2015_10
ORD IDord-c7631805aa824911971a003262873942
Source noteuspto-grants-2015_10