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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 930878Generated: October 31, 2026

Ammonia → 5-Bromo-6-chloropyridine-3-sulfonamide

https://huagongshe.com/reaction/930878

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant5-Bromo-6-chloropyridine-3-sulfonyl chlorideHCID 2793626—
SolventMethanolHCID 887—
Product5-Bromo-6-chloropyridine-3-sulfonamideHCID 4730022—

Reaction Steps

5-Bromo-6-chloropyridine-3-sulfonyl chloride (8.2 g) in methanol (20 mL) was cooled to 0° C. To this solution was added 7N NH3 in methanol (80 mL). The reaction mixture was stirred over night at room temperature. The solvent was removed at low temperature, and the residue was partitioned between ethyl acetate and water. The aqueous layer was extracted with ethyl acetate three times. The combined organic layers were washed with brine, dried (MgSO4), filtered, and concentrated. The solid was purified by flash column chromatography on silica gel to afford 4.2 g of the clean product.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09296741B2
Source datasetuspto-grants-2016_03
ORD IDord-34e0da58ca7f42e882d0895710724d89
Source noteuspto-grants-2016_03