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Chemical Structure| 89977-46-8 Chemical Structure| 89977-46-8

Structure of 89977-46-8

Chemical Structure| 89977-46-8

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Product Details of [ 89977-46-8 ]

CAS No. :89977-46-8
Formula : C8H8N4
M.W : 160.18
SMILES Code : NC1=CC=NN1C2=NC=CC=C2
MDL No. :MFCD11641441

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Application In Synthesis of [ 89977-46-8 ]

* 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 [ 89977-46-8 ]

[ 89977-46-8 ] Synthesis Path-Downstream   1~2

  • 1
  • [ 111771-08-5 ]
  • [ 89977-46-8 ]
  • [ 364726-76-1 ]
YieldReaction ConditionsOperation in experiment
64% EXAMPLE 2-162 4-Chloro-5-fluoro-1-(2-pyridinyl)-1H-pyrazolo[3,4-b]quinoline Following the procedures described in Reference Example 2-5 and Example 2-1, the title compound was prepared from <strong>[111771-08-5]2-fluoro-6-iodobenzoic acid</strong> and 1-(2-pyridinyl)-1H-pyrazol-5-ylamine (64% yield). mp: 173-176 C. (recrystallized from ethyl acetate). NMR (CDCl3) delta: 7.18-7.34 (2H, m), 7.66-7.79 (1H, m), 7.92-8.07 (2H, m), 8.62 (1H, s), 8.66-8.73 (2H, m).
  • 2
  • [ 13421-00-6 ]
  • [ 89977-46-8 ]
  • [ 364728-00-7 ]
YieldReaction ConditionsOperation in experiment
88% Reference Example 2-66 5-Chloro-2-[[1-(2-pyridinyl)-1H-pyrazol-5-yl]amino]<strong>[13421-00-6]benzoic acid</strong> Following the procedure described in Reference Example 2-5, the title compound was prepared from <strong>[13421-00-6]5-chloro-2-iodo<strong>[13421-00-6]benzoic acid</strong></strong> and 1-(2-pyridinyl)-1H-pyrazol-5-ylamine (88% yield). mp: 233-234 C. (recrystallized from ethanol). NMR (DMSO-d6) delta: 6.42 (1H, d, J=2.0 Hz), 7.38 (1H, ddd, J=1.2 Hz, 4.8 Hz, 7.4 Hz), 7.54 (1H, dd, J=2.6 Hz, 8.8 Hz), 7.63 (1H, d, J=8.8 Hz), 7.71 (1H, d, J=2.0 Hz), 7.88-7.92 (2H, m), 7.99-8.08 (1H, m), 8.47 (1H, dd, J=0.8 Hz, 1.8 Hz, 4.8 Hz), 12.24 (1H, br s), hidden (1H).
88% Production example 15 5-Chloro-2-[[1-(2-pyridinyl)-1H-pyrazol-5-yl]amino]<strong>[13421-00-6]benzoic acid</strong> Following the procedure described in Production Example 7, the title compound was prepared from <strong>[13421-00-6]5-chloro-2-iodo<strong>[13421-00-6]benzoic acid</strong></strong> and 1-(2-pyridinyl)-1H-pyrazol-5-ylamine (88% yield). mp: 233-234C (recrystallized from ethanol). NMR (DMSO-d6) delta: 6.42 (1H, d, J=2.0Hz), 7.38 (1H, ddd, J=1.2Hz, 4.8Hz, 7.4Hz), 7.54 (1H, dd, J=2.6Hz, 8.8Hz), 7.63 (1H, d, J=8.8Hz), 7.71 (1H, d, J=2.0Hz), 7.88-7.92 (2H, m), 7.99-8.08 (1H, m), 8.47 (1H, dd, J=0.8Hz, 1.8Hz, 4.8Hz), 12.24 (1H, br s), hidden (1H).
 

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