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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1670583Generated: October 30, 2026

Ammonium Hydroxide → 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide

https://huagongshe.com/reaction/1670583

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmonium HydroxideHCID 14923—
Reactant6-chloro-N-(1,3-thiazol-2-yl)pyridine-3-sulfonamideHCID 943191—
SolventEthanolHCID 702—
Product6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamideHCID 5755122122%

Reaction Conditions

Temperature120 °C

Reaction Steps

Under a N2 atmosphere, a mixture of 6-chloro-N-(thiazol-2-yl)pyridine-3-sulfonamide (0.7 g, 2.54 mmol), ammonium hydroxide (7.5 mL) and ethanol (7.5 mL), was stirred at 120° C. in a sealed tube for 4 days. The reaction was cooled to RT. After evaporating the solvents under reduced pressure, purification via silica gel chromatography using 5%-10% methanol in CH2Cl2 gave 6-amino-N-(thiazol-2-yl)pyridine-3-sulfonamide as a orange solid (0.14 g, 22%). LC/MS (10%-99% CH3CN (0.035% TFA)/H2O (0.05% TFA)), m/z: M+1 obs=257.2; tR=0.2 min.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07994174B2
Source datasetuspto-grants-2011_08
ORD IDord-64ae8275d387401298de2a6024ab768d
Source noteuspto-grants-2011_08