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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384376Generated: October 30, 2026

Sodium Bicarbonate → HCID 178435524, compound

https://huagongshe.com/reaction/384376

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant2-(3-Ethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 57483783—
Reactant3'-Amino-2'-hydroxy-biphenyl-3-carboxylic acid hydrobromideHCID 57483789—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178435524HCID 17843552436.4%

Reaction Steps

3′-Amino-2′-hydroxy-biphenyl-3-carboxylic acid hydrobromide 1f (285 mg, 0.92 mmol) was dissolved in 3.1 mL of hydrochloric acid (1 N) upon cooling by an ice-water bath, followed by dropwise addition of 1.2 mL of aqueous sodium nitrite (70 mg, 1.01 mmol). After the mixture was stirred for 20 minutes, 2-(3-ethyl-indan-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 41d (200 mg, 0.83 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 warmed up to room temperature overnight. 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. The mixture was filtered and the filter cake was dried to obtain the title compound 3′-{N′-[1-(3-ethyl-indan-5-yl)-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-2′-hydroxy-biphenyl-3-carboxylic acid 41 (145 mg, yield 36.4%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-9306d1c560ad4668afc3926e4a694efd
Source noteuspto-grants-2013_02