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Chemical Structure| 18818-41-2 Chemical Structure| 18818-41-2

Structure of 18818-41-2

Chemical Structure| 18818-41-2

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Product Details of [ 18818-41-2 ]

CAS No. :18818-41-2
Formula : C15H12N2O
M.W : 236.27
SMILES Code : O=C1NC(C2=CC=C(C)C=C2)=NC3=C1C=CC=C3
MDL No. :MFCD00446432

Safety of [ 18818-41-2 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H320-H335
Precautionary Statements:P261-P280-P301+P312-P302+P352-P305+P351+P338

Application In Synthesis of [ 18818-41-2 ]

* 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 [ 18818-41-2 ]

[ 18818-41-2 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 18818-41-2 ]
  • [ 51997-51-4 ]
  • 3-(3-((9H-carbazol-4-yl)oxy)-2-hydroxypropyl)-2-(p-tolyl)quinazolin-4(3H)-one [ No CAS ]
YieldReaction ConditionsOperation in experiment
80% With tetra-(n-butyl)ammonium iodide; potassium carbonate; In acetonitrile; at 80℃; for 36h;Inert atmosphere; General procedure: A mixture of 2-methyl quinazolin-4(3H)-one 3a (150 mg,0.937 mmol), <strong>[51997-51-4]4-(oxiran-2-ylmethoxy)-9H-carbazole</strong> (8, 222 mg,0.937 mmol), potassium carbonate (258 mg, 1.875 mmol) and tetrabutylammonium iodide (5 mg, 0.014 mol) were heated in acetonitrile (15 mL) at 80 C for 36 h under nitrogen atmosphere. The reaction mass was extracted with ethyl acetate, separated and the organic layer was dried over sodium sulfate and concentrated. The crude product was purified by column chromatography over silica gel (65:35, ethyl acetate/hexane) to give following compounds.
  • 2
  • [ 55577-25-8 ]
  • [ 18818-41-2 ]
YieldReaction ConditionsOperation in experiment
96% With ammonium hydroxide; oxygen; copper(I) bromide; In 1-methyl-pyrrolidin-2-one; at 60℃; for 30h; A solution of 2- (4-tolyl) -1H-indole in 0.25 mmol,Ammonia water 0.10g,0.0125 mmol of cuprous bromide,N-methylpyrrolidone 2.0 mL was added to 10 mL of the reaction tube,Placed in an oil bath at 60 C,Oxygen under the protection of 30h reaction.Stop the reaction,Cool to room temperature.The reaction solution was diluted with methylene chloride,Extracted three times with water,The organic phase was dried over anhydrous Na2SO4,filter,And 56.6 mg of the target product was isolated by column chromatography.The yield was 96%.
With ammonium hydroxide; oxygen; copper(I) bromide; In 1-methyl-pyrrolidin-2-one; at 80℃; for 24h; General procedure: A mixture of 2-arylindoles (0.25 mmol), ammonium hydroxide (0.10 g), and CuBr (5 mol %) in NMP (2 mL) was stirred at 80 C under oxygen for 24 h. After cooling to room temperature, the reaction mixture was poured into water and extracted with EtOAc. The organic layer was washed with brine, dried over MgSO4. Purification by column chromatography on silica gel using petroleum ether/ethyl acetate (10:1 to 5:1) as the eluent delivered the desired substrates.
 

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