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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25372생성일: 2026년 10월 23일

1H-Indazol-5-amine → 2-methylsulfonyl-N-(1H-indazol-5-yl)benzenesulfonamide

https://huagongshe.com/ko/reaction/25372

반응식

참여 물질

역할이름HCID투입량
반응물1H-Indazol-5-amineHCID 88012—
반응물2-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735178—
용매PyridineHCID 1049—
생성물2-methylsulfonyl-N-(1H-indazol-5-yl)benzenesulfonamideHCID 1172550224.3%

반응 단계

2-Methylsulfonyl-N-(1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 2 from 1 g of 5-amino-1H-indazole, 20 ml of pyridine and 1.91 g of 2-methylsulfonylbenzenesulfonyl chloride. 0.64 g of 2-methylsulfonyl-N-(1H-indazol-5-yl)benzenesulfonamide is thus obtained in the form of a white solid melting at 245° C. (analysis C14H13N3O4S2 % calculated C, 47.85; H, 3.73; N, 11.96; O, 18.21; S, 18.25. % found C, 47.42; H, 3.72; N, 11.64; S, 17.97).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858638B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a83dd8035d0c4a56966a660df1fb3a5b
출처 메모uspto-grants-2005_02