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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1095343Generated: October 31, 2026

Acetic Acid → HCID 16723510, compound

https://huagongshe.com/reaction/1095343

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAcetic AcidHCID 176—
ReactantAcetyl chlorideHCID 6367—
ReactantEthylhydrazineHCID 29062—
ReactantMethyl 3-indoleglyoxylateHCID 588944—
SolventEthanolHCID 702—
ProductHCID 16723510HCID 1672351034.5%

Reaction Steps

Acetyl chloride (0.7 mL, 9.8 mmol), acetic acid (1 mL), and ethylhydrazine (1.5 g, 9.8 mmol) were added sequentially to a suspension of methyl (1H-indol-3-yl)glyoxalate (1.0 g, 4.9 mmol) in ethanol (25 mL). The reaction mixture was heated at reflux for 18 hours. The reaction mixture was cooled to ambient temperature and then concentrated under reduced pressure. The residue was combined with acetonitrile. A pink solid was isolated by filtration and then purified by automated flash chromatography (Biotage, eluted with a gradient of 0-30% CMA in chloroform) to provide a white solid. This material was recrystallized from acetonitrile to provide 360 mg of 2-ethyl-2,5-dihydro-4H-pyrazolo[3,4-c]quinolin-4-one as white crystals, mp>250° C. MS (APCI) m/z 214 (M+H)+; Anal. calcd for C12H11N3O: C, 67.59; H, 5.20; N, 19.71. Found: C, 67.52; H, 5.14; N, 19.90.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08138173B2
Source datasetuspto-grants-2012_03
ORD IDord-dbb42cdfc7c849afbdcebaff2d4e491d
Source noteuspto-grants-2012_03