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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 25374생성일: 2026년 10월 23일

Tetrahydrofuran → 3-fluoro-N-(1H-indazol-5-yl)benzenesulfonamide

https://huagongshe.com/ko/reaction/25374

반응식

참여 물질

역할이름HCID투입량
반응물TetrahydrofuranHCID 8028—
반응물1H-Indazol-5-amineHCID 88012—
반응물3-Fluorobenzenesulfonyl ChlorideHCID 2734258—
용매TriethylamineHCID 8471—
생성물3-fluoro-N-(1H-indazol-5-yl)benzenesulfonamideHCID 366656936.6%

반응 단계

3-Fluoro-N-(1H-indazol-5-yl)benzenesulfonamide can be obtained as described in Example 1 from 0.4 g of 5-amino-1H-indazole, 20 ml of tetrahydrofuran, 0.83 ml of triethylamine and 0.88 g of 3-fluorobenzenesulfonyl chloride. 0.32 g of 3-fluoro-N-(1H-indazol-5-yl)-benzenesulfonamide is thus obtained in the form of a cream solid.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06858638B2
출처 데이터셋uspto-grants-2005_02
ORD IDord-a901e0ff14654107949f3e6221c794e7
출처 메모uspto-grants-2005_02