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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1419088Generated: November 1, 2026

Ethanol → HCID 53901480, compound

https://huagongshe.com/reaction/1419088

Reaction equation

Participants

RoleNameHCIDCharge
ReactantEthanolHCID 702—
Reactant4-Hydrazinylbenzenesulfonamide hydrochlorideHCID 2794567—
ReactantHCID 54244781HCID 54244781—
ProductHCID 53901480HCID 5390148030%

Reaction Steps

7-Methoxy-8-fluoro-3-(trifluoroacetyl)isochroman-4-one from Step 3 (450 mg, 1.47 mmol) and 4-sulfonamidophenylhydrazine hydrochloride (430 mg, 1.92 mmol) were dissolved in 5 mL of anhydrous ethanol and heated to reflux for 45 minutes. The solution was concentrated in vacuo and the residue was dissolved in ethyl acetate. The solution was washed with 3N hydrochloric acid, brine, dried over anhydrous MgSO4, filtered, and concentrated in vacuo. The residue was crystallized from a mixture of isooctane and ethyl acetate to afford 4-[1,4-dihydro-6-fluoro-7-methoxy-3-(trifluoromethyl)-[1]benzopyrano[4,3-c]pyrazol-1-yl]benzenesulfonamide as a white solid (200 mg, 30%): mp 289.5°-291.0° C.; 1H NMR (acetone d6 /300 MHz) 8.12 (d, J=8.4 Hz, 2H), 7.90 (d, J=8.5 Hz. 2H), 7.07 (dd, J=8.7, 8.5 Hz, 1H), 6.83 (br s, 2H), 6.75 (d, J=8.7 Hz, 1H), 5.45 (s, 2H), 3.90 (s, 3H); 19F NMR (acetone d6 /282 MHz) -62.51 (s), -140.97 (d). High resolution mass spectrum Calc'd. for C18H13F4N3O4S: 443.0563. Found: 443.0570.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05886016
Source datasetuspto-grants-1999_03
ORD IDord-79ecd1cd937246869a8c0e4558e8f482
Source noteuspto-grants-1999_03