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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25360생성일: 2026년 10월 25일

2-Methanesulfonylbenzene-1-sulfonyl chloride → N-(3-cyano-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide

https://huagongshe.com/reaction/25360

반응식

참여 물질

역할이름HCID투입량
반응물2-Methanesulfonylbenzene-1-sulfonyl chlorideHCID 2735178—
반응물5-Amino-1H-indazole-3-carbonitrileHCID 22567303—
용매PyridineHCID 1049—
생성물N-(3-cyano-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamideHCID 1004506311.5%

반응 단계

N-(3-Cyano-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide can be obtained as described in Example 2 from 0.55 g of 3-cyano-5-amino-1H-indazole, 10 ml of pyridine and 0.88 g of 2-methylsulfonylbenzenesulfonyl chloride. 0.15 g of N-(3-cyano-1H-indazol-5-yl)-2-methylsulfonylbenzenesulfonamide is thus obtained in the form of a yellow powder melting at 272° C. (analysis C15H12N4O4S2.0.85H2O, % calculated C, 47.87; H, 3.21; N, 14.88; S, 17.04. % found C, 47.88; H, 3.01; N, 14.75; S, 17.45).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858638B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-f83a3feddd8547ec88d94ae942a358e4
출처 메모uspto-grants-2005_02