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Chemical Structure| 50-97-5 Chemical Structure| 50-97-5

Structure of 50-97-5

Chemical Structure| 50-97-5

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Product Details of [ 50-97-5 ]

CAS No. :50-97-5
Formula : C14H12N2O
M.W : 224.26
SMILES Code : OC(C1=NC2=CC=CC=C2N1)C3=CC=CC=C3
MDL No. :MFCD00159953

Safety of [ 50-97-5 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319-H335
Precautionary Statements:P261-P264-P270-P271-P280-P301+P312-P302+P352-P304+P340-P305+P351+P338-P330-P332+P313-P337+P313-P362-P403+P233-P405-P501

Application In Synthesis of [ 50-97-5 ]

* 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 [ 50-97-5 ]

[ 50-97-5 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 3314-30-5 ]
  • [ 591-51-5 ]
  • [ 50-97-5 ]
  • 2
  • [ 13220-33-2 ]
  • [ 50-97-5 ]
  • [ 1370428-18-4 ]
YieldReaction ConditionsOperation in experiment
272A A mixture of (1 - -benzimidazol-2-yl)phenylmethanol (61 1 mg) and 1 -methyl-3- pyrrolidinol (263mg) in methanesulfonic acid (1 .3ml_) is heated for 4 hours in a sealed tube at a temperature close to 140°C. The mixture is cooled back to room temperature, poored into water which is then made alkaline with concentrated sodium hydroxyde solution. The aqueous phase is extracted with ethyl acetate. Pooled extracts are dried over magnesium sulfate, concentrated under reduced pressure. The residue is purified by column chromatography over silica gel (gradient dichloromethane/methanol from 100/0 to 90/10) to give 2-[(1 -methylpyrrolidin-3-yloxy)phenyl-methyl]-1 H-benzimidazole melting at 53 °C.For the other examples prepared according this general procedure, it can be a good idea to rise the temperature progressively after having mixed the different reagents and to observe when etherification occurs. Once the right temperature has been found, reaction is continued up to adequate conversion.
A mixture of (1H-benzimidazol-2-yl)phenylmethanol (611mg) and <strong>[13220-33-2]1-methyl-3-pyrrolidinol</strong> (263mg) in methanesulfonic acid (1.3mL) is heated for 4 hours in a sealed tube at a temperature close to 140°C. The mixture is cooled back to room temperature, poored into water which is then made alkaline with concentrated sodium hydroxyde solution. The aqueous phase is extracted with ethyl acetate. Pooled extracts are dried over magnesium sulfate, concentrated under reduced pressure. The residue is purified by column chromatography over silica gel (gradient dichloromethane/methanol from 100/0 to 90/10) to give 2-[(1-methylpyrrolidin-3-yloxy)phenyl-methyl]-1H-benzimidazole melting at 53°C.
 

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