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Chemical Structure| 163133-86-6 Chemical Structure| 163133-86-6

Structure of 163133-86-6

Chemical Structure| 163133-86-6

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Product Details of [ 163133-86-6 ]

CAS No. :163133-86-6
Formula : C4H5N3
M.W : 95.10
SMILES Code : N=C1N=CNC=C1

Safety of [ 163133-86-6 ]

Application In Synthesis of [ 163133-86-6 ]

* 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 [ 163133-86-6 ]

[ 163133-86-6 ] Synthesis Path-Downstream   1~5

  • 1
  • [ 53557-69-0 ]
  • [ 163133-86-6 ]
  • 2
  • [ 53557-69-0 ]
  • [ 7732-18-5 ]
  • zinc dust [ No CAS ]
  • [ 163133-86-6 ]
  • 3
  • [ 163133-86-6 ]
  • [ 51146-57-7 ]
  • 2-(4-isobutyl-phenyl)-<i>N</i>-pyrimidin-4-yl-propionamide [ No CAS ]
  • 4
  • [ 163133-86-6 ]
  • [ 27018-76-4 ]
  • [ 852059-74-6 ]
YieldReaction ConditionsOperation in experiment
Example 46 1-Benzyl-1H-indole-3-carboxylic acid pyrimidin-4-ylamide <strong>[27018-76-4]1-Benzylindole-3-carboxylic acid</strong> (25.9 mg, 96 mmol) was dissolved in SOCI2 (1 mL) and the mixture was stirred for 30 min before the volatiles were removed in vacuo. The residue was dissolved in MeCN (200 muL) and added to a solution of pyrimidin-4-yl-amine (10 mg, 105 mmol) in NMP (200 muL). The reaction mixture was stirred 16 hours at room temperature before the MeCN was removed in vacuo. The residue was purified using HPLC method D to give title compound. HPLC-MS (Method A): m/z = 329 (M+1); Rt = 3.3 min.
  • 5
  • [ 163133-86-6 ]
  • [ 34259-99-9 ]
  • N-(pyrimidine-4-yl)thiazol-4-amine [ No CAS ]
 

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