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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1875467Generated: October 27, 2026

4-Hydrazinobenzoic acid → 4-(3-oxo-1,3-dihydro-2H-pyrazolo[4,3-c]cinnolin-2-yl)benzoic acid

https://huagongshe.com/reaction/1875467

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Hydrazinobenzoic acidHCID 12089—
ReactantMethyl 4-chlorocinnoline-3-carboxylateHCID 20187472—
SolventEthanolHCID 702—
Product4-(3-oxo-1,3-dihydro-2H-pyrazolo[4,3-c]cinnolin-2-yl)benzoic acidHCID 58974914—

Reaction Conditions

Temperature47.5 °C

Reaction Steps

4-Hydrazinobenzoic acid (68.4 mg, 0.45 mmol) was mixed at room temperature with ethanol (5 ml) to give a crème-coloured suspension. Methyl 4-chlorocinnoline-3-carboxylate (100 mg, 0.45 mmol) was added and the mixture was heated to 45-50° C. for 1 h. The reaction mixture was cooled to room temperature and the solvent was removed under vacuum. Ethyl acetate (10 ml) was added to the residue. The mixture was stirred at room temperature for 1 h. The solids were collected by filtration and dried under vacuum. The title compound was isolated as a brown powder (120 mg, 0.39 mmol, 86%). LCMS: m/z 307 [M+H]+. NMR [DMSO-d6]: δ=7.69-7.77 (m, 1Haryl); 7.81-7.90 (m, 2Haryl); 8.05 (d, J=8.85, 2Haryl); 8.20 (d, J=7.92 Hz, 1Haryl); 8.33 (d, J=8.85 Hz, 2Haryl); 14.64 (s, NH).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08309552B2
Source datasetuspto-grants-2012_11
ORD IDord-ae32647676d9403896fefc92a0f0c1a8
Source noteuspto-grants-2012_11