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Chemical Structure| 1613335-06-0 Chemical Structure| 1613335-06-0

Structure of 1613335-06-0

Chemical Structure| 1613335-06-0

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Product Details of [ 1613335-06-0 ]

CAS No. :1613335-06-0
Formula : C15H15BrN2O2
M.W : 335.20
SMILES Code : O=C(N1C=C(CC#N)C2=C1C=C(Br)C=C2)OC(C)(C)C
MDL No. :MFCD32876058

Safety of [ 1613335-06-0 ]

GHS Pictogram:
Signal Word:Warning
Hazard Statements:H302-H315-H319
Precautionary Statements:P501-P270-P264-P280-P302+P352-P337+P313-P305+P351+P338-P362+P364-P332+P313-P301+P312+P330

Application In Synthesis of [ 1613335-06-0 ]

* 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 [ 1613335-06-0 ]

[ 1613335-06-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 1613335-06-0 ]
  • [ 82257-15-6 ]
  • [ 1613334-70-5 ]
YieldReaction ConditionsOperation in experiment
35% General procedure: Method F: Synthesis of (Z)-2-(6-X-lH-indol-3-yl)-3-(4-methoxypyridin-3- yl)acrylonitrile To a solution of tert-butyl 6-X-3-(cyanomethyl)-lH-indole-l-carboxylate(l eq) in THF, was added NaH (eq). The resulting mixture was stirred 10 min at room temperature and <strong>[82257-15-6]4-methoxynicotinaldehyde</strong> (1.3 eq) was added with one drop of DMF. The mixture was stirred at room temperature hidden from light. The reaction was quenched with aqueous NH4C1 and extracted with AcOEt, dried over Na2S04, filtrated and concentrated. The residue was dissolved with THF and NaOH 2.5 M was added. The system was stirred at room temperature hidden from light, diluted with AcOEt, dried over Na2S04, filtrated and concentrated. The residue was taken off with a minimal amount of AcOEt and filtrated to give the title compound.
 

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