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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384296Generated: October 31, 2026

Sodium Bicarbonate → HCID 178433805, compound

https://huagongshe.com/reaction/384296

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acidHCID 21072315—
ReactantSodium NitriteHCID 23668193—
Reactant2-Indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-oneHCID 57483780—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433805HCID 17843380515.3%

Reaction Steps

Upon cooling by an ice-water bath, 3′-amino-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid 2f (296 mg, 1.20 mmol) was dissolved in 10 mL of hydrochloric acid (1 N) followed by addition of 10 mL of aqueous sodium nitrite (91 mg, 1.32 mmol) and 2-indan-5-yl-5-methyl-2,4-dihydro-pyrazol-3-one 1i (257 mg, 1.20 mmol). The mixture was adjusted to pH 8 with saturated aqueous sodium bicarbonate, followed by addition of 10 mL of ethanol. The 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, dried and recrystallized from methanol to obtain the title compound 5′-fluoro-2′-hydroxy-3′-[N′-(1-indan-5-yl-3-methyl-5-oxo-1,5-dihydro-pyrazol-4-ylidene)-hydrazino]-biphenyl-3-carboxylic acid 2 (87 mg, yield 14.1%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-67f52718da41400a860b7f87ef5b0aa4
Source noteuspto-grants-2013_02