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Chemical Structure| 22426-18-2 Chemical Structure| 22426-18-2

Structure of 22426-18-2

Chemical Structure| 22426-18-2

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Product Details of [ 22426-18-2 ]

CAS No. :22426-18-2
Formula : C12H9N3
M.W : 195.22
SMILES Code : NC1=NC2=C3N=CC=CC3=CC=C2C=C1
MDL No. :MFCD03838356

Safety of [ 22426-18-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 22426-18-2 ]

* All experimental methods are cited from the reference, please refer to the original source for details. We do not guarantee the accuracy of the content in the reference.

  • Downstream synthetic route of [ 22426-18-2 ]

[ 22426-18-2 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 7089-68-1 ]
  • [ 22426-18-2 ]
YieldReaction ConditionsOperation in experiment
94% With acetamide; potassium carbonate; at 200℃; for 5h; <strong>[7089-68-1]2-Chloro-1,10-phenanthroline</strong> (100 mg, 0.5 mmol) and potassiumcarbonate (451 mg, 3.3 mmol) and acetamide (688 mg,11.7 mmol) were stirred at 200 C for 5 h. The reaction mixturewas cooled to room temperature, and poured into water. The aqueouslayer was extracted with chloroform (40 mL) twice. The combinedorganic layers were washed with brine and dried overmagnesium sulfate. The crude product was purified by silica gelchromatography eluted with chloroform/methanol = 100:1 to give2 (85 mg, 94%) as white solids.
52.5% With acetamide; potassium carbonate; at 200℃; for 1h; <strong>[7089-68-1]2-chloro-1,10-phenanthroline</strong> (859 mg, 4 mmol), acetamide (4.73 g, 80 mmol), potassium carbonate (3.87 g, 28 mmol), and heated to 200 C, stirred for 1 hour, dropped to room temperature, add water (30 mL) to the reaction and extract with dichloromethane. The organic phase was collected, dried over anhydrous sodium sulfate and filtered. The organic phase was removed by concentration under reduced pressure. The residue was subjected to silica gel column chromatography to afford 2-amino-1,10-phenanthroline 409 mg (2.1 mmol, 52.5%).
 

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