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HRID 1634286作成日:2026年10月27日

2-Sulfamyl-5-acetylamino-pyridine → 5-Aminopyridine-2-sulfonamide

https://huagongshe.com/reaction/1634286

反応式

関与物質

役割名称HCID仕込み量
反応物2-Sulfamyl-5-acetylamino-pyridineHCID 22499579—
溶媒Sodium HydroxideHCID 14798—
生成物5-Aminopyridine-2-sulfonamideHCID 2231385070%

反応手順

N-(6-Mercapto-pyridin-3-yl)-acetamide (30 g, 17.3 mmol) was dissolved in cold concentrated hydrochloric acid solution (225 ml), followed by the addition of ice water (50 ml). Chlorine was bubbled into solution, and the temperature was kept below 10° C. The solution became dark brown first, and the chlorination was complete after 3 hours when the temperature no longer rose and the color of the solution lightened. The reaction was diluted with ice and water (1.2 kg) while keeping the temperature below 10° C. The product, 5-acetylamino-pyridine-2-sulfonyl chloride, was collected by filtration and air-dried. This was then suspended in chloroform (CHCl3) (200 mL), followed by the addition of 30% ammonia solution (100 ml), and the resulting reaction mixture was stirred for 2 hours. The solvent was removed in vacuo to give a black solid, 2-sulfamyl-5-acetylamino-pyridine. 2-Sulfamyl-5-acetylamino-pyridine was dissolved in 0.85 N NaOH solution (500 ml), and the resulting solution was stirred at refluxing temperature for 3.5 hours. After cooled down to room temperature, the reaction mixture was extracted with 3:1 of CHCl3/MeOH solution (3×200 ml). The aqueous layer was neutralized to pH 7, and water was removed in vacuo to give the crude product which was recrystallized from water to afford the title compound (21.6 g, 70%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06506779B1
出典データセットuspto-grants-2003_01
ORD IDord-317e73838bd34861af255dd59666ac95
出典メモuspto-grants-2003_01