Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384355Generated: October 26, 2026

Sodium Bicarbonate → HCID 178433835, compound

https://huagongshe.com/reaction/384355

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant2-(3,3-Dimethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 51036994—
Reactant3'-Amino-2'-hydroxy-biphenyl-3-carboxylic acid hydrobromideHCID 57483789—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433835HCID 178433835115.1%

Reaction Steps

3′-Amino-2′-hydroxy-biphenyl-3-carboxylic acid hydrobromide 1f (310 mg, 1.0 mmol) was dissolved in hydrochloric acid (3.4 mL, 1 mol/L) upon cooling by an ice-water bath, followed by dropwise addition of 1.2 mL of aqueous sodium nitrite (73 mg, 1.05 mmol). After the mixture was reacted for 10 minutes, 2-(3,3-dimethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 8i (218 mg, 0.9 mmol), sodium bicarbonate (1.26 g, 15 mmol) and 4.4 mL of ethanol were added successively. The reaction mixture was reacted at room temperature for 10 hours. The reaction was monitored by TLC until the disappearance of the starting materials. The mixture was filtered and the filter cake was washed with 20 mL of water and then dissolved in 20 mL of water. Upon cooling by an ice-water bath, the mixture was adjusted to pH<5 with concentrated hydrochloric acid, filtered and dried to obtain the title compound 3′-{N′-[1-(3,3-dimethyl-indan-5-yl)-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-2′-hydroxy-biphenyl-3-carboxylic acid 30 (500 mg, yield 94%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-a38f1ec6b54a49c2b649997e392c24b9
Source noteuspto-grants-2013_02