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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1943947Generated: November 2, 2026

Sodium nitromalonaldehyde hydrate → HCID 178427406, compound

https://huagongshe.com/reaction/1943947

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium nitromalonaldehyde hydrateHCID 71317419—
ReactantHCID 178427407HCID 178427407—
ReactantHCID 178461063HCID 178461063—
SolventAcetic AcidHCID 176—
SolventWaterHCID 962—
ProductHCID 178427406HCID 17842740663.8%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08394795B2
Source datasetuspto-grants-2013_03
ORD IDord-8eefbc4964684a86a9f856bb44a582ca
Source noteuspto-grants-2013_03