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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384298Generated: October 26, 2026

Sodium Bicarbonate → HCID 178433808, compound

https://huagongshe.com/reaction/384298

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodium BicarbonateHCID 516892—
ReactantSodium NitriteHCID 23668193—
Reactant3-Methyl-1-(5,6,7,8-tetrahydronaphthalen-2-yl)-1H-pyrazol-5(4H)-oneHCID 51036580—
Reactant3'-Amino-2'-hydroxy-biphenyl-3-carboxylic acid hydrobromideHCID 57483789—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433808HCID 17843380811.6%

Reaction Steps

Upon cooling by an ice-water bath, 3′-amino-2′-hydroxy-biphenyl-3-carboxylic acid hydrobromide 1f (250 mg, 1.09 mmol) was dissolved in 10 mL of hydrochloric acid (1 N) followed by addition of 10 mL of aqueous sodium nitrite (82 mg, 1.2 mmol) and 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 3i (249 mg, 1.09 mmol). Then 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. 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 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 3 (59 mg, yield 11.6%) as a yellow solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-5b88644628874ab998773c82842cb156
Source noteuspto-grants-2013_02