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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1520640Generated: November 3, 2026

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

https://huagongshe.com/reaction/1520640

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 mixture was added 7N NH3 in methanol (80 mL). The reaction mixture was stirred overnight. 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 using 10-50% ethyl acetate in hexanes to give the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09073855B2
Source datasetuspto-grants-2015_07
ORD IDord-09e97495c1e841e6a3b7e9b681c47cf2
Source noteuspto-grants-2015_07