HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 588272Generated: October 29, 2026
Sulfuric Acid → 5-(1-phenyl-1H-pyrazol-5-yl)indolin-2-one
https://huagongshe.com/reaction/588272
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sulfuric Acid | HCID 1118 | — |
| Reactant | Phenylhydrazine | HCID 7516 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 90417345 | HCID 90417345 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 5-(1-phenyl-1H-pyrazol-5-yl)indolin-2-one | HCID 90417801 | 42.1% |
Reaction Steps
To a solution of 5-(3,3-diethoxyprop-1-ynyl)indolin-2-one (100 mg, 0.39 mmol) in acetonitrile (5 ml) were added phenyl hydrazine (38 μL, 0.38 mmol) and sulfuric acid (52 μL, 0.98 mmol), and the mixture was stirred for 3 h at room temperature, then the mixture was stirred for 2 h at 50° C. The reaction mixture was poured into water (50 mL), and the resulting precipitate was filtered and dried. The precipitated was dissolved in acetonitrile (5 mL), then water (52 μL, 3.9 mmol) and sulfuric acid (93 μL, 1.75 mmol) were added. The mixture was heated at 80 C for 4 h. The mixture was cooled to room temperature, and then neutralized with sat. NaHCO3. The mixture was extracted with CHCl3/EtOAc 3 times. The combined organic extracts were washed with sat. NaCl, dried over Na2SO4, and evaporated in vacuo. The residue purified by column chromatography (EtOAc/n-hexane) to give the title compound as a brown solid (44 mg, 41%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09227962B2 |
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| Source dataset | uspto-grants-2016_01 |
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| ORD ID | ord-789a5e75e1a8482cb753c94eb7d01643 |
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| Source note | uspto-grants-2016_01 |
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