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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1941703생성일: 2026년 10월 27일

4-Hydrazinylbenzenesulfonamide hydrochloride → 4-[4,5-Dihydro-7-methyl-3-(trifluoromethyl)-1h-benz[g]indazol-1-yl]benzenesulfonamide

https://huagongshe.com/reaction/1941703

반응식

참여 물질

역할이름HCID투입량
반응물4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
반응물6-Methyl-2-(trifluoroacetyl)tetraloneHCID 22315552—
용매EthanolHCID 702—
생성물4-[4,5-Dihydro-7-methyl-3-(trifluoromethyl)-1h-benz[g]indazol-1-yl]benzenesulfonamideHCID 1208282064%

반응 단계

4-Sulfonamidophenylhydrazine hydrochloride (1.80 g, 8.0 mmol) was added to a stirred solution of the diketone from Step 1 (1.86 g, 7.3 mmol) in ethanol (10 mL). The reaction was heated to reflux and stirred for 14.8 hours. The reaction mixture was cooled and filtered. The filtrate was concentrated in vacuo, dissolved in ethyl acetate, washed with water and with brine, dried over MgSO4 and reconcentrated in vacuo to give the pyrazole as a brown solid (1.90 g, 64%): mp 215°-218° C. 1H NMR (acetone-d6) 300 MHz 8.10 (d, 2H), 7.80 (d, 2H), 7.24 (s, 1H), 6.92 (d, 1H), 6.79 (br s, 2H), 6.88 (d,1H), 3.02 (m, 2H), 2.85 (m, 2H), 2.30 (s, 3H). 19F NMR (acetone-d6) 282 MHz −62.46 (s). High resolution mass spectrum Calc'd. for C19H17F3O2S: 408.0994. Found: 408.0989.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호USRE044048E1
출처 데이터셋uspto-grants-2013_03
ORD IDord-90dd72c571e345528e4c6706ba1be763
출처 메모uspto-grants-2013_03