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Chemical Structure| 17286-62-3 Chemical Structure| 17286-62-3

Structure of 17286-62-3

Chemical Structure| 17286-62-3

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Product Details of [ 17286-62-3 ]

CAS No. :17286-62-3
Formula : C15H12N2
M.W : 220.27
SMILES Code : CC1=CC=C(C2=NC3=CC=CC=C3N=C2)C=C1

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Application In Synthesis of [ 17286-62-3 ]

* 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 [ 17286-62-3 ]

[ 17286-62-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 4079-54-3 ]
  • [ 95-54-5 ]
  • [ 17286-62-3 ]
YieldReaction ConditionsOperation in experiment
90% With gallium(III) perchlorate; In ethanol; at 25℃; General procedure: Representative experimental procedure for the synthesis of 2-phenylquinoxaline (3a) (Table 2, entry 1): A mixture of o-phenylenediamine (1a, 0.0541 g, 0.5 mmol), 2-hydroxyaceto-phenone (2a, 0.0681 g, 0.5 mmol) and Ga(ClO4)3 (0.018g, 0.05 mmol) in EtOH (3 mL) was stirred at room temperature. The progress of the reaction was monitored by TLC. After completion of the reaction, the mixture was directly purified by silica gel column chromatography (petroleum ether/ethyl acetate, 10:1) to afford the product 3a. The structures of all products were confirmed by IR, 1H NMR spectroscopy and melting points, which were consistent with literature data.
70% With triphenylantimony; In toluene; at 20℃; for 3h; General procedure: Triphenylstibane(35.5 mg, 0.1 mmol, 10 mol%) and diamine 2 (1.2 mmol) were added to a solution of -hydroxy ketone 1(1 mmol) in toluene (6 mL) under air. The solution was stirred at room temperature and monitored byTLC. The reaction mixture was concentrated under reduced pressure and the residue was purified bycolumn chromatography (CH2Cl2) on silica gel. The products were confirmed by comparison of mp,NMR data, and MS spectra with that in the literature. 822:
  • 2
  • [ 4079-54-3 ]
  • [ 88-74-4 ]
  • [ 17286-62-3 ]
 

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