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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 858483Generated: November 1, 2026

1H-pyrazole-3-carbaldehyde → HCID 178487281, compound

https://huagongshe.com/reaction/858483

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1H-pyrazole-3-carbaldehydeHCID 12218383—
ReactantHCID 21876179HCID 21876179—
ReactantHCID 178418268HCID 178418268—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
ProductHCID 178487281HCID 17848728116.1%

Reaction Steps

A mixture of 2-(4-{[2-amino-4-(methyloxy)phenyl]amino}phenyl)ethanol (step 2 of Example 71, 1.95 g, 7.56 mmol), pyrazol-3-carbaldehyde (726 mg, 7.56 mmol) in ethanol (45 ml) was heated at reflux temperature for 2 h. After cooling, the mixture was concentrated. A mixture of the residue, lead tetraacetate (4.61 g, 8.32 mmol) in benzene (50 ml) was stirred at room temperature for 16 h. The mixture was quenched with saturated NaHCO3 aqueous solution (150 ml). The whole was extracted with ethyl acetate (150 ml×4). The organic layer was washed with water (100 ml×5), brine (50 ml), dried (MgSO4), and concentrated. Purification by flash column chromatography eluting with dichloromethane/methanol (gradient elution from 20:1 to 10:1) to afford 408 mg (16%) of the title compound as an amber solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS07148234B2
Source datasetuspto-grants-2006_12
ORD IDord-00faabaa4e5c493d916bfe4e7d3af3fd
Source noteuspto-grants-2006_12