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Chemical Structure| 893620-48-9 Chemical Structure| 893620-48-9

Structure of 893620-48-9

Chemical Structure| 893620-48-9

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Product Details of [ 893620-48-9 ]

CAS No. :893620-48-9
Formula : C8H7NO
M.W : 133.15
SMILES Code : O=CC1=CC=CN=C1C=C
MDL No. :MFCD06654833

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Application In Synthesis of [ 893620-48-9 ]

* 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 [ 893620-48-9 ]

[ 893620-48-9 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 893620-48-9 ]
  • [ 138006-41-4 ]
  • [ 936011-14-2 ]
YieldReaction ConditionsOperation in experiment
With n-butyllithium; In tetrahydrofuran; hexane; di-isopropyl ether; at -78℃; for 0.5h; To a stirred solution of nBuLi (1.6 M in hexane, 5.5 mL, 8.8 mL) in diisopropyl ether (20 mL) was added <strong>[138006-41-4]3-bromo-2,5-dichloropyridine</strong> (2.0 g, 8.8 mmol) in diisopropylether (10 mL) slowly at - 78 0C. The resulting suspension was treated with 2-vinylnicotinaldehyde (1.2 g, 8.8 mmol) in THF (5 mL) and allowed to stir for 30 min at -78 0C followed by warming to room temperature. The mixture was diluted with EtOAc, washed with water and brine, dried (Na2SO4), concentrated, and purified by flash chromatography to afford the title compound. 1H NMR (600 MHz, CDCl3) delta 8.58 (dd, IH); 8.32 (d, IH); 7.83 (d, IH); 7.54 (dd, IH); 7.21 (dd, IH); 7.06 (dd, IH); 6.42 (dd, IH); 6.37 (br s, IH); 5.58 (dd, IH); 2.79 (br s, IH). LRMS (ESI) calc'd for (C13H10Cl2N2O) [M+H]+, 281.0; found 280.7.
With n-butyllithium; In tetrahydrofuran; hexane; di-isopropyl ether; at -78℃; for 0.5h; Step 2: (2,5-dichloropyridin-3-yl)(2-vinylpyridin-3-yl)methanol; To a stirred solution of nBuLi (1.6 M in hexane, 5.5 mL, 8.8 mL) in diisopropyl ether (20 mL) was added 3-bromo-2,5-dichlororhoyridine (2.0 g, 8.8 mmol) in diisopropylether (10 mL) slowly at - 78 0C. The resulting suspension was treated with 2-vinylnicotinaldehyde (1.2 g, 8.8 mmol) in THF (5 mL) and allowed to stir for 30 min at -78 0C followed by warming to room temperature. The mixture was diluted with EtOAc, washed with water and brine, dried (Na2SO4), concentrated, and purified by flash chromatography to afford the title compound. 1H NMR (600 MHz, CDCl3) delta 8.58 (dd, IH); 8.32 (d, IH); 7.83 (d, IH); 7.54 (dd, IH); 7.21 (dd, IH); 7.06 (dd, IH); 6.42 (dd, IH); 6.37 (br s, IH); 5.58 (dd, IH); 2.79 (br s, IH). LRMS (ESI) calc'd for (C13HiOCl2N2O) [M+H]+, 281.0; found 280.7.
 

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