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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384333Generated: October 29, 2026

Sodium Bicarbonate → HCID 178433811, compound

https://huagongshe.com/reaction/384333

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant3-Methyl-1-(5,6,7,8-tetrahydronaphthalen-2-yl)-1H-pyrazol-5(4H)-oneHCID 51036580—
Reactant5-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromideHCID 57483805—
SolventHydrochloric AcidHCID 313—
ProductHCID 178433811HCID 17843381139.8%

Reaction Steps

5-(3-Amino-2-hydroxy-phenyl)-furan-2-carboxylic acid hydrobromide 9c (292 mg, 0.975 mmol) was dissolved in 3.3 mL of hydrochloric acid (1 N) upon cooling by an ice-water bath, followed by dropwise addition of 1.3 mL of aqueous sodium nitrite (74 mg, 1.07 mmol). After the mixture was stirred for 20 minutes, 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 3i (200 mg, 0.88 mmol) was added. The mixture was adjusted to pH 8-9 by batch addition of aqueous sodium bicarbonate (1.226 g, 14.6 mmol). The generated bubbles were quenched with 2 mL of ethanol. The reaction mixture was warmed up to room temperature and reacted overnight. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was dissolved in 20 mL of water. After mixing well, the mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid, filtered and dried. The crude product was purified by HPLC to obtain the title compound 5-(2-hydroxy-3-{N′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthalen-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-phenyl)-furan-2-carboxylic acid 15 (160 mg, yield 39.8%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-61ad07e00bf44cd69011b392a48dfbbf
Source noteuspto-grants-2013_02