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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 384361Generated: October 30, 2026

Sodium Bicarbonate → HCID 178433828, compound

https://huagongshe.com/reaction/384361

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—
Reactant5-(3-Amino-2-hydroxy-5-methyl-phenyl)-thiophene-2-carboxylic acid hydrobromideHCID 57483821—
SolventHydrochloric AcidHCID 313—
SolventEthanolHCID 702—
ProductHCID 178433828HCID 17843382818.09%

Reaction Steps

5-(3-Amino-2-hydroxy-5-methyl-phenyl)-thiophene-2-carboxylic acid hydrobromide 24d (366 mg, 1.11 mmol) was dissolved in 3.7 mL of 1 N hydrochloric acid upon cooling by an ice-water bath, followed by dropwise addition of 1.5 mL of aqueous sodium nitrite (85 mg, 1.22 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 (228 mg, 1 mmol), sodium bicarbonate (1.4 g, 16.67 mmol) and 2 mL of ethanol were added successively. 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 30 mL of water. The mixture was adjusted to pH 3˜4 with concentrated hydrochloric acid. The mixture was filtered and the filter cake was dried and purified by silica gel column chromatography to obtain the title compound 5-(2-hydroxy-5-methyl-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 33 (88 mg, yield 18.09%) as a red solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08367710B2
Source datasetuspto-grants-2013_02
ORD IDord-6c3f0dadba754edbb526fbb9d14f4a2e
Source noteuspto-grants-2013_02