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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2227419Generated: October 25, 2026

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

https://huagongshe.com/reaction/2227419

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
Reactant6-Methyl-2-(trifluoroacetyl)tetraloneHCID 22315552—
SolventEthanolHCID 702—
Product4-[4,5-Dihydro-7-methyl-3-(trifluoromethyl)-1h-benz[g]indazol-1-yl]benzenesulfonamideHCID 1208282064%

Reaction Steps

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 C19H17F3N3O2S: 408.0994. Found: 408.0989.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06413960B1
Source datasetuspto-grants-2002_07
ORD IDord-ac34caf46ebf4a5f805a6c0c216bbad2
Source noteuspto-grants-2002_07