HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384356Generated: October 29, 2026
Sodium Bicarbonate → HCID 178433798, compound
https://huagongshe.com/reaction/384356
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | Sodium Nitrite | HCID 23668193 | — |
| Reactant | 2-Indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one | HCID 57483780 | — |
| Reactant | 4-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide | HCID 57483826 | — |
| Solvent | Hydrochloric Acid | HCID 313 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 178433798 | HCID 178433798 | 36.7% |
Reaction Steps
4-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide 28e (170 mg, 0.57 mmol) was dissolved in hydrochloric acid (1.9 mL, 1 mol/L) upon cooling by an ice-water bath, followed by dropwise addition of 0.7 mL of aqueous sodium nitrite (43 mg, 0.63 mmol). After the mixture was reacted for 20 minutes, 2-indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one 1i (109 mg, 0.51 mmol) was added. The mixture was adjusted to pH 8˜9 with saturated aqueous sodium bicarbonate, followed by addition of 2 mL of ethanol. The reaction mixture was reacted at room temperature for 24 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and 15 mL of water was added to the filter cake. Upon cooling by an ice-water bath, the mixture was adjusted to pH 2˜3 with concentrated hydrochloric acid, filtered and the filter cake was washed with ethyl acetate, and then dried to obtain the title compound 4-{2-hydroxy-3-[N′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-phenyl}-furan-2-carboxylic acid 31 (83 mg, yield 36.7%) as a black solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08367710B2 |
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| Source dataset | uspto-grants-2013_02 |
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| ORD ID | ord-d12c19096f614e4da6b1bc68d4776591 |
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| Source note | uspto-grants-2013_02 |
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