HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943947Generated: November 2, 2026
Sodium nitromalonaldehyde hydrate → HCID 178427406, compound
https://huagongshe.com/reaction/1943947
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium nitromalonaldehyde hydrate | HCID 71317419 | — |
| Reactant | HCID 178427407 | HCID 178427407 | — |
| Reactant | HCID 178461063 | HCID 178461063 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 178427406 | HCID 178427406 | 63.8% |
Reaction Steps
Nitromalonaldehyde sodium salt monohydrate (3.57 g, 22.7 mmol) was added to suspension of 5-amino-1-tosyl-1H-pyrazol-3-ol (5.00 g, 19.7 mmol; see Elgemeie, Galal H., et al. “Novel Synthesis of 5-Amino-1-arylsulfonyl-4-pyrazolin-3-ones as a New Class of N-Sulfonylated Pyrazoles.” J. Chem. Res. (S). Issue 6 (1999): pp. 384-385) in acetic acid (30 mL). The mixture was heated at 50° C. for 4 hours. The partial suspension was allowed to cool and diluted with water. The resulting solid was collected by vacuum filtration and dried under high vacuum to afford 5-nitro-1-tosyl-1H-pyrazolo[3,4-b]pyridin-3-ol (4.21 g, 12.6 mmol, 63.8% yield) as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08394795B2 |
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| Source dataset | uspto-grants-2013_03 |
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| ORD ID | ord-8eefbc4964684a86a9f856bb44a582ca |
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| Source note | uspto-grants-2013_03 |
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