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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1639613Generated: October 25, 2026

5,6-Dimethoxy-2-(4-nitro-1,2-dihydro-3H-pyrazol-3-ylidene)-2H-benzimidazole → HCID 178486794, compound

https://huagongshe.com/reaction/1639613

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5,6-Dimethoxy-2-(4-nitro-1,2-dihydro-3H-pyrazol-3-ylidene)-2H-benzimidazoleHCID 178486795—
CatalystPalladiumHCID 23938—
SolventEthanolHCID 702—
SolventDimethylformamideHCID 6228—
ProductHCID 178486794HCID 17848679453.6%

Reaction Steps

A mixture of 5,6-dimethoxy-2-(4-nitro-1H-pyrazol-3-yl)-1H-benzimidazole (2.08 g, 7.2 mmol) and 10% palladium on carbon (200 mg) in ethanol (150 ml) and DMF (50 ml) was hydrogenated at room temperature and pressure overnight. The reaction mixture was filtered through Celite and the solvent removed in vacuo. The resulting solid was azeotroped with methanol and toluene and the solvent removed in vacuo. The crude material was purified by flash chromatography, eluting with DCM:MeOH:acetic acid:water (120:18:3:2) [DMAW120] followed by DCM:MeOH:acetic acid:water (90:18:3:2) (DMAW90). Product fractions were combined and the solvent removed in vacuo to yield 3-(5,6-dimethoxy-1H-benzimidazol-2-yl)-1H-pyrazol-4-ylamine (˜1 g, 53%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08110573B2
Source datasetuspto-grants-2012_02
ORD IDord-931ab2be03c44f99b8e4c8b707d5b4fc
Source noteuspto-grants-2012_02