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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384399Generated: October 30, 2026

Sodium Bicarbonate → HCID 178433800, compound

https://huagongshe.com/reaction/384399

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)-thiophene-2-carboxylic acid hydrobromideHCID 57483846—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433800HCID 17843380028.7%

Reaction Steps

4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 51c (120 mg, 0.38 mmol) was dissolved in 2.7 mL of 1 N hydrochloric acid upon cooling by an ice-water bath, followed by dropwise addition of 0.45 mL of aqueous sodium nitrite (29 mg, 0.42 mmol). After the mixture was reacted for 20 minutes, 2-indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one 1i (73 mg, 0.34 mmol) was added. The mixture was adjusted to pH 8 with saturated aqueous sodium bicarbonate followed by addition of 2 mL of ethanol. The reaction mixture was reacted overnight at room temperature. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was added to 20 mL of water. The mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid and filtered. Then 5 mL of ethyl acetate was added to the filter cake and the mixture was stirred for 1 hour. The mixture was filtered and the filter cake was 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}-thiophene-2-carboxylic acid 52 (45 mg, yield 28.7%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-0cd32a1b85484d00b9f4523f2f4d2d96
Source noteuspto-grants-2013_02