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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 724125Generated: November 1, 2026

Hydrochloric Acid → HCID 178487281, compound

https://huagongshe.com/reaction/724125

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHydrochloric AcidHCID 313—
Reactant1H-pyrazole-3-carbaldehydeHCID 12218383—
ReactantHCID 21876179HCID 21876179—
ReactantHCID 178418268HCID 178418268—
SolventBenzeneHCID 241—
SolventEthanolHCID 702—
SolventMethanolHCID 887—
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 1.37 mmol) in methanol (4 ml) was added 10% HCl in methanol (2 ml) at room 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 numberUS07141580B2
Source datasetuspto-grants-2006_11
ORD IDord-9a7fdb2d16994c10b8bd382942d85b1d
Source noteuspto-grants-2006_11