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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384332Generated: October 29, 2026

Sodium Bicarbonate → HCID 178433846, compound

https://huagongshe.com/reaction/384332

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant2-(2,3-Dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 57483781—
Reactant3'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acid hydrochlorideHCID 57483816—
SolventHydrochloric AcidHCID 313—
ProductHCID 178433846HCID 17843384620%

Reaction Steps

3′-Amino-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid hydrochloride 2f (219 mg, 0.772 mmol) was dissolved in 3 mL of hydrochloric acid (1 N) upon cooling by an ice-water bath, followed by dropwise addition of 1 mL of aqueous sodium nitrite (59 mg, 0.85 mmol). After the mixture was stirred for 20 minutes, 2-(2,3-dihydro-benzofuran-5-yl)-5-methyl-2,4-dihydro-pyrazol-3-one 7c (150 mg, 0.69 mmol) was added. The mixture was adjusted to pH 8˜9 by batch addition of aqueous sodium bicarbonate (1.007 g, 11.57 mmol). The generated bubbles were quenched with 2 mL of ethanol. 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 15 mL of water. After mixing well, the mixture 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 3′-{N′-[1-(2,3-dihydro-benzofuran-5-yl)-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid 14 (65 mg, yield 20.0%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-d6decd527a0c41c09fd28a9586f7e539
Source noteuspto-grants-2013_02