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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 369082생성일: 2026년 10월 23일

4-Hydrazinylbenzenesulfonamide hydrochloride → 4-[5-(6-chlorobenzothiazol-2-yl)-3-trifluoromethyl-1H-pyrazol-1-yl]benzenesulfonamide

https://huagongshe.com/ko/reaction/369082

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
반응물4,4,4-Trifluoro-1-(6-chlorobenzothiazol-2-yl)butane-1,3-dioneHCID 23285375—
생성물4-[5-(6-chlorobenzothiazol-2-yl)-3-trifluoromethyl-1H-pyrazol-1-yl]benzenesulfonamideHCID 23285420—

반응 단계

The procedure of Example 9 was repeated using 4,4,4-trifluoro-1-(6-chlorobenzothiazol-2-yl)butane-1,3-dione and 4-sulfamoylphenylhydrazine hydrochloride as the starting materials to obtain 4-[5-(6-chlorobenzothiazol-2-yl)-3-trifluoromethyl-1H-pyrazol-1-yl]benzenesulfonamide. NMR(CDCl3 -DMSO-d6) δ: 6.91 (2H, bs), 7.30-7.49 (2H, m), 7.63 (2H, d, J=8.9 Hz), 7.88-7.91 (2H, m), 8.05 (2H, d, J=8.9 Hz); mp 254-255° C. (ethanol)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US06136831
출처 데이터셋uspto-grants-2000_10
ORD IDord-c274906ee8e74ad28bcd35a3ed1c5375
출처 메모uspto-grants-2000_10