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HRID 962846Erstellt: 24. Oktober 2026

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

https://huagongshe.com/de/reaction/962846

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
Edukt6-Methyl-2-(trifluoroacetyl)tetraloneHCID 22315552—
LösungsmittelEthanolHCID 702—
Produkt4-[4,5-Dihydro-7-methyl-3-(trifluoromethyl)-1h-benz[g]indazol-1-yl]benzenesulfonamideHCID 1208282064%

Reaktionsschritte

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.

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05760068
Quelldatensatzuspto-grants-1998_06
ORD IDord-44658100d2ba4ee69dd990db3cf58bfa
Quellennotizuspto-grants-1998_06