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Chemical Structure| 1350516-03-8 Chemical Structure| 1350516-03-8

Structure of 1350516-03-8

Chemical Structure| 1350516-03-8

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Product Details of [ 1350516-03-8 ]

CAS No. :1350516-03-8
Formula : C16H14N2
M.W : 234.30
SMILES Code : CCC1=CC=C(C2=NC3=CC=CC=C3N=C2)C=C1
MDL No. :N/A

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Application In Synthesis of [ 1350516-03-8 ]

* 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 [ 1350516-03-8 ]

[ 1350516-03-8 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 2632-14-6 ]
  • [ 95-54-5 ]
  • [ 1350516-03-8 ]
YieldReaction ConditionsOperation in experiment
92% With potassium fluoride on basic alumina; at 20℃; for 2h; General procedure: A mixture of 1,2-diamine (1 mmol) and alpha-bromo ketone (1 mmol) was intimately mixed with pre-activated KF-alumina (1:4) (0.5 g) (Basic; Grade: Brockmann 1, and activated by heating under vacuum at 150 C until bubbling ceases and then cooled to room temperature under vacuum) and stirred the solid mixture with a magnetic spin bar at room temperature for hours as indicated in refPreviewPlaceHolderTable 3. After the reaction was complete, the solid mixture washed with diethyl ether (3 × 10 mL) and the solid was filtered off. The filtrate was concentrated and passed through a short column of silica gel to afford the quinoxalines. The desired product was pure on TLC and characterized by spectral (1H and 13C NMR) data and compared to those reported.
With polymeric resin-bound hexafluorophosphate ion; In methanol; water; at 20℃; for 6h; General procedure: In a typical experimental procedure, o-phenlylenediamine and alpha-bromo ketone in 1:1 molar ratios was taken in a 100 mL round bottom flask. To this water-methanol (1:1) and 100 mg PHP was admixed. The reaction mixture was then allowed to stir with magnetic spinning bar, after some time a yellowish mass appeared which settles down like a precipitate after the completion of the reaction (checked by TLC). It was then filtered; the solid reaction mixture was dissolved with dichloromethane (25 mL) and evaporated under vacuum. The crude product was then crystallised from ethanol. The desired product was pure on TLC and characterized by spectral (IR, 1H and 13C NMR) data and compared to those reported in literature.
 

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