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Chemical Structure| 691856-35-6 Chemical Structure| 691856-35-6

Structure of 691856-35-6

Chemical Structure| 691856-35-6

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Product Details of [ 691856-35-6 ]

CAS No. :691856-35-6
Formula : C20H19FN2O4S
M.W : 402.44
SMILES Code : O=C(C1=C(C2=CC=C(F)C=C2)OC3=CC(NS(=O)(C)=O)=C(C4CC4)C=C13)NC

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Application In Synthesis of [ 691856-35-6 ]

* 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 [ 691856-35-6 ]

[ 691856-35-6 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 691856-35-6 ]
  • [ 2106-50-5 ]
  • [ 1423007-28-6 ]
YieldReaction ConditionsOperation in experiment
64% With potassium carbonate; In 1,2-dimethoxyethane; water; at 20 - 100℃; for 88h;Sealed tube; Step 1 : 6-(N-(3-Chloro-4-nitrophenyl)methylsulfonamido)-5-cyclopropyl-2-(4-fluorophenyl)- N-methylbenzofuran-3-carboxamide A mixture of 5-cyclopropyl-2-(4-fluorophenyl)-N-methyl-6-(methylsulfonamido)benzofuran- 3-carboxamide (12.5 g , 31.1 mmol), <strong>[2106-50-5]2-chloro-4-fluoronitrobenzene</strong> (10.9 g, 62.1 mmol) and potassium carbonate (12.9 g, 93.0 mmol) in 130 mL of 4:1 DME/water in a sealed flask was heated to 100C with stirring. An identical 12.5 g scale reaction was set up in a second sealed vessel. The reaction vessels were maintained at 100C for 70 hours, cooled to RT, and stirred for an additional 18 hours. The combined reaction mixtures were partitioned between EtOAc (300 mL) and water (600 mL), and the phases separated. The aqueous solution was extracted with two additional 150 mL portions of EtOAc. The combined EtOAc solutions were washed with half saturated brine (1 x), saturated brine (1x), dried over sodium sulfate and concentrated to dryness at reduced pressure. The resulting yellow-brown solid was recrystallized from EtOAc/ether to give the title compound (22.3 g, 64%) as an off-white solid. LCMS {m/z, ES+) = 558 (M+H+).
64% With potassium carbonate; In 1,2-dimethoxyethane; water; at 100℃; for 70h;Sealed tube; Step 1 : 6-(N-(3-Chloro-4-nitrophenyl)methylsulfonamido)-5-cyclopmethylbenzofuran-3-carboxamide A mixture of 5-cyclopropyl-2-(4-fluorophenyl)-N-methyl-6-(methylsulfonamido)benzofuran-3- carboxamide (12.5 g , 31 .1 mmol), <strong>[2106-50-5]2-chloro-4-fluoronitrobenzene</strong> (10.9 g, 62.1 mmol) and potassium carbonate (12.9 g, 93.0 mmol) in 130 ml. of 4:1 DME/water in a sealed flask was heated to 100C with stirring. An identical 12.5 g scale reaction was set up in a second sealed vessel. The reaction vessels were maintained at 100C for 70 hours, cooled to RT, and stirred for an additional 18 hours. The combined reaction mixtures were partitioned between EtOAc (300 ml.) and water (600 ml_), and the phases separated. The aqueous solution was extracted with two additional 150 ml. portions of EtOAc. The combined EtOAc solutions were washed with half saturated brine (1 x), saturated brine (1 x), dried over sodium sulfate and concentrated to dryness at reduced pressure. The resulting yellow-brown solid was recrystallized from EtOAc/ether to give the title compound (22.3 g, 64%) as an off-white solid. LCMS {m/z, ES+) = 558 (M+H+).
  • 2
  • [ 691856-35-6 ]
  • [ 51323-43-4 ]
  • [ 1331942-27-8 ]
 

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