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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384354Generated: November 1, 2026

Sodium Bicarbonate → HCID 178433802, compound

https://huagongshe.com/reaction/384354

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant2-Indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 57483780—
Reactant3'-Amino-2'-hydroxy-5'-methyl-biphenyl-3-carboxylic acid hydrochlorideHCID 57483809—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433802HCID 17843380215%

Reaction Steps

3′-Amino-2′-hydroxy-5′-methyl-biphenyl-3-carboxylic acid hydrochloride 11f (346 mg, 1.07 mmol) was dissolved in hydrochloric acid (5 mL, 2 mol/L) upon cooling by an ice-water, followed by addition of 2 mL of aqueous sodium nitrite (81 mg, 1.17 mmol). After the mixture was reacted for 30 minutes, 2-indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one 1i (229 mg, 1.07 mmol) was added. The mixture was adjusted to pH 8 with saturated aqueous sodium bicarbonate, followed by addition of 5 mL of ethanol. The 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 washed with ethanol. The filtrate was poured into a mixture of ice and water. The resulting mixture was adjusted to pH 4 with concentrated hydrochloric acid to form precipitates. The mixture was filtered and the filter cake was washed three times with ethyl acetate, and then dried to obtain the title compound 2′-hydroxy-3′-[N′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-5′-methyl-biphenyl-3-carboxylic acid 29 (75 mg, yield 15%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-09bd99817e77498f992a8eea0c487a60
Source noteuspto-grants-2013_02