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Chemical Structure| 27393-85-7 Chemical Structure| 27393-85-7

Structure of 27393-85-7

Chemical Structure| 27393-85-7

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Product Details of [ 27393-85-7 ]

CAS No. :27393-85-7
Formula : C16H12N2
M.W : 232.28
SMILES Code : C(N1)(C2=CNC3=C2C=CC=C3)=CC4=C1C=CC=C4
MDL No. :MFCD00225372

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Application In Synthesis of [ 27393-85-7 ]

* 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 [ 27393-85-7 ]

[ 27393-85-7 ] Synthesis Path-Downstream   1~3

  • 1
  • [ 3616-56-6 ]
  • [ 27393-85-7 ]
  • [ 111296-91-4 ]
YieldReaction ConditionsOperation in experiment
67% With acetic acid; at 118℃; for 8h;Inert atmosphere; Under a nitrogen atmosphere, 14.1 g (0.061 mol) of the intermediate A, 11.4 g (0.071 mol) ofN,N'-<strong>[3616-56-6]dimethylaminoacetaldehyde diethyl acetal</strong>, and 110.0 g of acetic acid were stirred for 8 hours while being heated at 118°C to reflux. After the reaction solution was cooled to room temperature, the precipitated crystal was collected by filtration and washed with acetic acid (30 ml) . The resultant crystal was subjected to purification by reslurrying to afford 10.4 g (67percent yield) of IC-2 as a white crystal.
67% With acetic acid; at 118℃; for 8h;Inert atmosphere; Under a nitrogen atmosphere, 14.1 g (0.061 mol) of Intermediate C, 11.4 g (0.071 mol) of N,N?-<strong>[3616-56-6]dimethylaminoacetaldehyde diethyl acetal</strong>, and 110.0 g of acetic acid were stirred for 8 hr while being refluxed under heat at 118° C. After the reaction solution had been cooled to room temperature, the precipitated crystal was taken by filtration and washed with acetic acid (30 ml). The resultant crystal was subjected to re-slurry purification to provide 10.4 g (0.041 mol, yield: 67percent) of 5,12-dihydroindolo[3,2-a]carbazole (IC-5) as a white crystal.
60% With acetic acid; at 130℃;Inert atmosphere; (3) 1H,1'H-2,3'-biindole (16.4 g, 70.6 mmol) and 2,2-diethoxy-N,N-dimethylethanamine (14.18 ml, 78 mmol) in glacial acetic acid (160 mL) were refluxed at 130 °C overnight under nitrogen. The reaction solution was cooled to room temperature and filtered. The filtrate was washed with small amount of acetic acid and excess of water. The filtrate was dried in the oven at 65°C overnight affording 10.79 g (60percent) of the 5,12-dihydroindolo[3,2-a]carbazole as gray solid.
  • 2
  • [ 15121-84-3 ]
  • [ 120-72-9 ]
  • [ 27393-85-7 ]
  • 3
  • [ 3616-56-6 ]
  • [ 27393-85-7 ]
  • C18H14N2 [ No CAS ]
YieldReaction ConditionsOperation in experiment
91% With acetic acid; for 6h; 1) 1H, 1'H-2, 3'-twoversus(dimethylamino)Acetaldehyde acetalAccording to the molar ratio of 1:1 to 3,Stir in acetic acid for 6 hours.Rearrangement to obtain an intermediate with a yield of 91%
 

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