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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384336Generated: October 30, 2026

Sodium Bicarbonate → HCID 178433796, compound

https://huagongshe.com/reaction/384336

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant2-Indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 57483780—
Reactant5-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromideHCID 57483814—
SolventHydrochloric AcidHCID 313—
ProductHCID 178433796HCID 1784337963.3%

Reaction Steps

5-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 12c (380 mg, 1.2 mmol) was dissolved in 3.9 mL of hydrochloric acid (1 N) upon cooling by an ice-water bath, followed by dropwise addition of 1.5 mL of aqueous sodium nitrite (90 mg, 1.32 mmol). After the mixture was stirred for 20 minutes, 2-indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one 1i (210 mg, 1 mmol) was added. The mixture was adjusted to pH 8˜9 by batch addition of aqueous sodium bicarbonate (1.51 g, 18 mmol). The generated bubbles were quenched with 2 mL of ethanol and 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 5% aqueous sodium hydroxide. The layers were separated and then the aqueous layer was extracted with dichloromethane (50 mL×3). The aqueous layer 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′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-phenyl}-thiophene-2-carboxylic acid 18 (15 mg, yield 3.3%) as an orange solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-a7a701d3eac6476cab9c1eaa041c4511
Source noteuspto-grants-2013_02