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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384398Generated: October 29, 2026

Sodium Bicarbonate → HCID 178433824, compound

https://huagongshe.com/reaction/384398

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—
Reactant4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromideHCID 57483846—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433824HCID 17843382410.2%

Reaction Steps

4-(3-Amino-2-hydroxy-phenyl)-thiophene-2-carboxylic acid hydrobromide 51c (80 mg, 0.25 mmol) was dissolved in 1 mL of 1 N hydrochloric acid upon cooling by an ice-water bath, followed by dropwise addition of 0.3 mL of aqueous sodium nitrite (19 mg, 0.28 mmol). After the mixture was reacted for 20 minutes, 5-methyl-2-(5,6,7,8-tetrahydro-naphthalen-2-yl)-2,4-dihydro-pyrazol-3-one 3i (52 mg, 0.23 mmol) was added. The mixture was adjusted to pH 8 with saturated aqueous sodium bicarbonate followed by addition of 2 mL of ethanol. The reaction 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 added to 20 mL of water. The mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid. The mixture was filtered and 4 mL of ethyl acetate was added to the filter cake. The resulting mixture was stirred for 2 hours and filtered, the filter cake was dried to obtain the title compound 4-(2-hydroxy-3-{N′-[3-methyl-5-oxo-1-(5,6,7,8-tetrahydro-naphthalen-2-yl)-1,5-dihydro-pyrazol-4-ylidene]-hydrazino}-phenyl)-thiophene-2-carboxylic acid 51 (11 mg, yield 10.2%) as a black solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-b4709ba7775c49259aeaafbddb303b1c
Source noteuspto-grants-2013_02