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Chemical Structure| 148887-61-0 Chemical Structure| 148887-61-0

Structure of 148887-61-0

Chemical Structure| 148887-61-0

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Product Details of [ 148887-61-0 ]

CAS No. :148887-61-0
Formula : C16H9Cl2NO2
M.W : 318.15
SMILES Code : O=C(C1=CC(C2=CC=C(Cl)C(Cl)=C2)=NC3=CC=CC=C13)O
MDL No. :MFCD01414694

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Application In Synthesis of [ 148887-61-0 ]

* 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 [ 148887-61-0 ]

[ 148887-61-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 148887-61-0 ]
  • [ 1597-32-6 ]
  • [ 1208372-52-4 ]
YieldReaction ConditionsOperation in experiment
9.53% With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In dichloromethane; at 20℃;Cooling with ice; 4-carboxylic acid (INT-1 ; 7.000 g, 22.0016 mmol) and 2-amino-6-fluoropyhdine (2.467 g, 22.0016 mmol) in dichloromethane (200 ml), triethylamine (15.584 g, -21.5 ml, 154.0112 mmol) is added, followed by portion-wise addition of 1 - propanephosphonic acid cyclic anhydride (37.803 g, 59.4043 mmol) and the mixture is allowed to attain room temperature spontaneously overnight. The resulting mixture is concentrated (-100 ml), washed with water and brine, dried (MgSO4), and evaporated to afford a brown gummy residue (9.100 g, 100% mass balance). This is purified by column chromatography eluting with 8% ethyl acetate in hexane, to obtain the title compound as an orange solid (0.865 g, 9.53% yield). M.p. 204.2-205.50C.
9.53% With 2,4,6-tripropyl-1,3,5,2,4,6-trioxatriphosphinane-2,4,6-trioxide; triethylamine; In dichloromethane; at 20℃;Cooling with ice; To a stirred and ice-cooled solution of 2-(3,4-dichloro-phenyl)-quinoline-4-carboxylic acid (INT-1; 7.000 g, 22.0016 mmol) and <strong>[1597-32-6]2-amino-6-fluoropyridine</strong> (2.467 g, 22.0016 mmol) in dichloromethane (200 ml), triethylamine (15.584 g, 21.5 ml, 154.0112 mmol) is added, followed by portion-wise addition of 1-propanephosphonic acid cyclic anhydride (37.803 g, 59.4043 mmol) and the mixture is allowed to attain room temperature spontaneously overnight. The resulting mixture is concentrated (100 ml), washed with water and brine, dried (MgSO4), and evaporated to afford a brown gummy residue (9.100 g, 100% mass balance). This is purified by column chromatography eluting with 8% ethyl acetate in hexane, to obtain the title compound as an orange solid (0.865 g, 9.53% yield). M.p. 204.2-205.5 C
 

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