돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 548382생성일: 2026년 10월 24일

Ethyl Acetate → 3-Aminopyridine-2-sulfonamide

https://huagongshe.com/ko/reaction/548382

반응식

참여 물질

역할이름HCID투입량
반응물Ethyl AcetateHCID 8857—
반응물Ammonium ChlorideHCID 25517—
반응물3-Nitropyridine-2-sulfonamideHCID 1201511—
촉매IronHCID 23925—
용매EthanolHCID 702—
생성물3-Aminopyridine-2-sulfonamideHCID 1494370276.3%

반응 조건

온도105 °C

반응 단계

3-Nitro-pyridine-2-sulfonic acid amide (3 g, 14.77 mmol) and iron powder (5 g, <10 micron) were suspended in ethanol (100 mL). Saturated aqueous ammonium chloride solution (60 mL) was added and the mixture stirred at 105° C. for 1.5 h. Upon cooling to 25° C., ethyl acetate (200 mL) was added and the mixture was shaken vigorously. The entire mixture was filtered through a plug of Celite. The resulting filtrate was diluted with ethyl acetate (100 mL) and the layers were separated. The aqueous layer was back-extracted with ethyl acetate (3×200 mL). The organic layers were combined, dried over magnesium sulfate, filtered and concentrated in vacuo to dryness. The resulting solid was triturated with a 3:1 mixture of hexanes and ethyl acetate (˜10 mL). The solid was collected by vacuum filtration and dried in vacuo for 16 h to afford the desired product, 3-amino-pyridine-2-sulfonic acid amide (1.95 g, 11.27 mmol, 76%), as an off-white powder. 1H NMR (400 MHz, DMSO-d6) δ: 5.98 (2H, bs), 7.19-7.21 (1H, m), 7.32 (2H, bs), 7.79-7.80 (1H, m), 7.90-7.91 (1H, m).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07939524B2
출처 데이터셋uspto-grants-2011_05
ORD IDord-04f09e8d78e24e43be34dd44a60a200d
출처 메모uspto-grants-2011_05