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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384299Generated: October 31, 2026

Sodium Bicarbonate → HCID 178433829, compound

https://huagongshe.com/reaction/384299

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
Reactant3'-Amino-5'-fluoro-2'-hydroxy-biphenyl-3-carboxylic acidHCID 21072315—
ReactantSodium NitriteHCID 23668193—
Reactant3-Methyl-1-(5,6,7,8-tetrahydronaphthalen-2-yl)-1H-pyrazol-5(4H)-oneHCID 51036580—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433829HCID 17843382913.1%

Reaction Steps

Upon cooling by an ice-water bath, 3′-amino-5′-fluoro-2′-hydroxy-biphenyl-3-carboxylic acid 2f (250 mg, 1.01 mmol) was dissolved in 10 mL of hydrochloric acid (1 N) followed by addition of 10 mL of aqueous sodium nitrite (77 mg, 1.12 mmol) and 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 4i (230 mg, 1.01 mmol). The mixture was adjusted to pH 8 with saturated aqueous sodium bicarbonate, followed by addition of 10 mL of ethanol. The reaction was warmed up to room temperature overnight and 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′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthalen-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-biphenyl-3-carboxylic acid 4 (64 mg, yield 13.1%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-0767224f66574e67bd6d980515277809
Source noteuspto-grants-2013_02