Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Acetyl chloride | HCID 6367 | — |
| Reactant | Ethylhydrazine | HCID 29062 | — |
| Reactant | Methyl 3-indoleglyoxylate | HCID 588944 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 16723510 | HCID 16723510 | 34.5% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08138173B2 |
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| Source dataset | uspto-grants-2012_03 |
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| ORD ID | ord-dbb42cdfc7c849afbdcebaff2d4e491d |
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| Source note | uspto-grants-2012_03 |
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