Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Acetic Acid | HCID 176 | — |
| Reactant | Phthalic Anhydride | HCID 6811 | — |
| Reactant | 5-Amino-1H-pyrazol-3-ol | HCID 96221 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 178514959 | HCID 178514959 | — |
Reaction Steps
To a solution of 3-amino-1H-pyrazol-5-ol (10.00 g, 101 mmol) in THF (300 mL) at RT was added phthalic acid anhydride (14.9 g, 101 mmol) followed by acetic acid (69.3 ml, 1.21 mol). The mixture was heated to reflux. After 4 days, the mixture was concentrated in vacuo to afford a slurry that was cooled to 0° C. and filtered. The solid was rinsed with Et2O and dried in vacuo to afford 2-(5-hydroxy-1H-pyrazol-3-yl)isoindoline-1,3-dione as a yellow solid that was advanced without further purification. MS: Found M+H+=230.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08404694B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-2c128b4fcd084ed586a683b37ed74654 |
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| Source note | uspto-grants-2013_03 |
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