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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384356Generated: October 29, 2026

Sodium Bicarbonate → HCID 178433798, compound

https://huagongshe.com/reaction/384356

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant2-Indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 57483780—
Reactant4-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromideHCID 57483826—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433798HCID 17843379836.7%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-d12c19096f614e4da6b1bc68d4776591
Source noteuspto-grants-2013_02