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Chemical Structure| 1428799-33-0 Chemical Structure| 1428799-33-0

Structure of 1428799-33-0

Chemical Structure| 1428799-33-0

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Product Details of [ 1428799-33-0 ]

CAS No. :1428799-33-0
Formula : C11H12N2O
M.W : 188.23
SMILES Code : O=C1NC2=C(C=CC=N2)C13CCCC3
MDL No. :MFCD31697820

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Application In Synthesis of [ 1428799-33-0 ]

* 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 [ 1428799-33-0 ]

[ 1428799-33-0 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 110-52-1 ]
  • [ 5654-97-7 ]
  • [ 1428799-33-0 ]
YieldReaction ConditionsOperation in experiment
0.1 g To stirred solution of 7-Azaoxindole 1(0.5 g ,3.73mmol ) in anhydrous THF(10 ml ) was added n-butyl lithium (0.47g,7.42 mmol)at -78C followed by TMEDA(0.865 g, 7.42mmol). After lh ,1,4dibromobutane (0.571 g, 3.73 mmol ) was added slowly and mixture was allowed to come up to room temperature. After stirring for 15h, saturated aqueous ammonium chloride was added and the crude material was partitioned between water and ethyl acetate. Organic layer was separated, dried over sodium sulphate and concentrated under vacuum. Crude compound was purified by column chromatography by eluting with 50% ethyl acetate in pet ether to get the desired compound 2 (0.1 g)
0.1 g Step-1 [0059] To stirred solution of 7-Azaoxindole 1 (0.5 g, 3.73 mmol) in anhydrous THF (10 ml) was added n-butyl lithium (0.47 g, 7.42 mmol) at -78 C. followed by TMEDA (0.865 g, 7.42 mmol). After 1 h, 1,4 dibromobutane (0.571 g, 3.73 mmol) was added slowly and mixture was allowed to come up to room temperature. After stirring for 15 h, saturated aqueous ammonium chloride was added and the crude material was partitioned between water and ethyl acetate. Organic layer was separated, dried over sodium sulphate and concentrated under vacuum. Crude compound was purified by column chromatography by eluting with 50% ethyl acetate in pet ether to get the desired compound 2 (0.1 g)
 

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