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Chemical Structure| 849217-54-5 Chemical Structure| 849217-54-5

Structure of 849217-54-5

Chemical Structure| 849217-54-5

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Product Details of [ 849217-54-5 ]

CAS No. :849217-54-5
Formula : C12H10F3NO5S
M.W : 337.27
SMILES Code : O=S(C(F)(F)F)(OC1=CC=NC2=CC(OC)=C(OC)C=C12)=O
MDL No. :MFCD26127249

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Application In Synthesis of [ 849217-54-5 ]

* 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 [ 849217-54-5 ]

[ 849217-54-5 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 849217-54-5 ]
  • [ 849217-60-3 ]
  • [ 849217-68-1 ]
YieldReaction ConditionsOperation in experiment
44% With 2,6-dimethylpyridine; at 165℃; for 18h;Sealed tube; 6,7-Dimethoxyquinolin-4-yl trifluoromethanesulfonate (5 g, 14.8 mmol) was added to a solution ofN- (4-fluorophenyl) -N '- (4-hydroxyphenyl) -cyclopropane-1,1-dicarboxamide (6.98 g, 22.2 mmol)2,6-lutidine (50 ml).The reaction mixture was stirred in a borning jar at 165 C for 18 hours.The reaction mixture was evaporated to dryness under reduced pressure and the remaining solid was dissolved in dichloromethane (250 ml)Wash twice with aqueous sodium hydroxide (1 N).The crude product was passed through a column of solid N- [4 - [(6,7-dimethoxy-Quinolyl) oxy] phenyl] -N '- (4-fluorophenyl) -1,1- cyclopropane dicarboxamide (3.2 g, yield: 44%),Captopinib
44% With 2,6-dimethylpyridine; at 165℃; for 18h; To a solution of cyclopropane-l, L-DICARBOXYLIC acid (4- fluoro-phenyl) -amide (4-hydroxy-phenyl) -amide (6.98 g, 22.2 mmol) in anhydrous 2,6- lutidine (50 mL) was added trifluoromethanesulfonic acid 6,7-dimethoxy-quinolin-4-yl ester (5 g, 14.8 mmol). The reaction mixture was heated at 165C in a sealed pressure tube with stirring for 18 h. The reaction mixture was concentrated on high vacuum to completely remove lutidine. The resulting solid material was dissolved in DCM (250 mL), and washed several times with 1 N sodium hydroxide to remove the excess phenol. The crude mixture was loaded on a silica gel flash column and eluted with 75% EtOAc- hexanes, affording N- (4- { [6,7-bis (methyloxy) quinolin-4-yl] OXY} PHENYL)-N- (4- fluorophenyl) cyclopropane-l, L-DICARBOXAMIDE (3.2 g, 44%).
 

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