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Chemical Structure| 390357-42-3 Chemical Structure| 390357-42-3

Structure of 390357-42-3

Chemical Structure| 390357-42-3

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Product Details of [ 390357-42-3 ]

CAS No. :390357-42-3
Formula : C15H12Br2N2
M.W : 380.08
SMILES Code : BrC1=CC=C2N3CC4=CC(Br)=CC=C4N(C3)CC2=C1

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Application In Synthesis of [ 390357-42-3 ]

* 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 [ 390357-42-3 ]

[ 390357-42-3 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 952514-79-3 ]
  • [ 390357-42-3 ]
  • 2,8-bis(4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocine [ No CAS ]
YieldReaction ConditionsOperation in experiment
51.5% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In ethanol; water; toluene; for 24h;Reflux; Toluene (40ml),To a mixed solution of EtOH (20 ml) and water (20 ml)2,8-dibromo-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocine(0.82 g, 2.16 mmol), <strong>[952514-79-3](4-(1-phenyl-1H-benzo[d]imidazol-2-yl)phenyl)boronic acid</strong>(1.5 g, 4.77 mmol), tetrakis (triphenylphosphine) palladium (0)(0.25 g, 0.216 mmol),potassium carbonate(0.90 g, 6.51 mmol) And refluxed for 24 hours.After cooling the reaction solution,The solvent was removed by decompression.DichloromathaneAnd the organic layer was separated After drying with sodium sulfate (anhydrous) The solvent was removed by decompression.The solid product (0.84 g, 51.5%) was obtained by column chromatography with hexane: acetone = 1: 1.
  • 2
  • [ 867044-33-5 ]
  • [ 390357-42-3 ]
  • 2,8-bis(4-(2-phenyl-1H-benzo[d]imidazol-1-yl)phenyl)-6,12-dihydro-5,11-methanodibenzo[b,f][1,5]diazocine [ No CAS ]
YieldReaction ConditionsOperation in experiment
63% With tetrakis(triphenylphosphine) palladium(0); potassium carbonate; In 1,4-dioxane; water; at 110℃; for 24h; To a mixed solution of dioxane (80 ml) and water (10 ml)2,8-dibromo-6,12-dihydro-5,11-methanodibenzo [b, f] [1,5] diazocine(1.00 g, 2.63 mmol),(4- (2-phenyl-1H-benzo [d] imidazol-1-yl) phenyl) boronic acid(2.07 g, 6.58 mmol),tetrakis (triphenylphosphine) palladium (0)(0.15 g, 0.132 mmol), (1.45 g, 10.52 mmol) was added thereto and refluxed for 24 hours.After cooling the reaction solution,The solvent was removed by decompression.After extraction with dichloromathane, the organic layer was separated and dried with sodium sulfate (anhydrous)The solvent was removed by decompression.Hexane: Ethyl Acetate = 2: 1 to obtain a solid product (1.26 g, 63%).
 

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