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HRID 962846作成日:2026年10月26日

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

https://huagongshe.com/reaction/962846

反応式

関与物質

役割名称HCID仕込み量
反応物4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
反応物6-Methyl-2-(trifluoroacetyl)tetraloneHCID 22315552—
溶媒EthanolHCID 702—
生成物4-[4,5-Dihydro-7-methyl-3-(trifluoromethyl)-1h-benz[g]indazol-1-yl]benzenesulfonamideHCID 1208282064%

反応手順

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 C19H17F3 O2S: 408.0994. Found: 408.0989.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05760068
出典データセットuspto-grants-1998_06
ORD IDord-44658100d2ba4ee69dd990db3cf58bfa
出典メモuspto-grants-1998_06