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Chemical Structure| 367521-07-1 Chemical Structure| 367521-07-1

Structure of 367521-07-1

Chemical Structure| 367521-07-1

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Product Details of [ 367521-07-1 ]

CAS No. :367521-07-1
Formula : C6H5Br2NO
M.W : 266.92
SMILES Code : OC1=CC(N)=C(Br)C=C1Br
MDL No. :MFCD01318097

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Application In Synthesis of [ 367521-07-1 ]

* 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 [ 367521-07-1 ]

[ 367521-07-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 13721-01-2 ]
  • [ 367521-07-1 ]
  • N-(2,4-dibromo-5-hydroxyphenyl)-4-oxo-1,4-dihydroquinoline-3-carboxamide [ No CAS ]
YieldReaction ConditionsOperation in experiment
With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 85℃; for 2h; To a 100-mL round-bottom flask was placed a solution of 4-oxo-l,4-dihydroquinoline-3- carboxylic acid (945 mg, 5.00 mmol) in DMF (25 mL) then 5-amino-2,4-dibromophenol (1.99 g, 7.46 mmol, as prepared in the previous step), HATU (3.8 g, 9.99 mmol), and DIEA (2 g, 15.48 mmol) were added. The reaction was stirred for 2 days at 85C then diluted with 100 mL of water and extracted with EtOAc (3x200 mL). The organic extracts were combined and concentrated under reduced pressure. The crude product was triturated with EtOAc affording 1.1 g of the title compound as a white solid. Mass Spectrum (LCMS, ESI pos): Calcd. for Ci6HiiBr2N203+: 436.9 (M+H); Found: 437.1.
1.1 g With N-ethyl-N,N-diisopropylamine; N-[(dimethylamino)-3-oxo-1H-1,2,3-triazolo[4,5-b]pyridin-1-yl-methylene]-N-methylmethanaminium hexafluorophosphate; In N,N-dimethyl-formamide; at 85℃; for 48h; To a 100-mL round-bottom flask was placed a solution of 4-oxo-l,4- dihydroquinoline-3-carboxylic acid (945 mg, 5.00 mmol) in DMF (25 mL) then 5-amino-2,4- dibromophenol (1.99 g, 7.46 mmol, as prepared in the previous step), HATU (3.8 g, 9.99 mmol), and DIEA (2 g, 15.48 mmol) were added. The reaction was stirred for 2 days at 85°C then diluted with 100 mL of water and extracted with EtOAc (3x200 mL). The organic extracts were combined and concentrated under reduced pressure. The crude product was triturated with EtOAc affording 1.1 g of the title compound as a white solid. Mass Spectrum (LCMS, ESI pos): Calcd. for Ci6HnBr2N203+: 436.9 (M+H); Found: 437.1.
 

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