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Chemical Structure| 54526-01-1 Chemical Structure| 54526-01-1

Structure of 54526-01-1

Chemical Structure| 54526-01-1

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Product Details of [ 54526-01-1 ]

CAS No. :54526-01-1
Formula : C10H10BrNO4
M.W : 288.10
SMILES Code : O=C(C1C(CBr)=CC=CC=1[N+](=O)[O-])OCC

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Application In Synthesis of [ 54526-01-1 ]

* 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 [ 54526-01-1 ]

[ 54526-01-1 ] Synthesis Path-Downstream   1~1

  • 1
  • [ 608141-42-0 ]
  • [ 54526-01-1 ]
  • [ 1227368-31-1 ]
YieldReaction ConditionsOperation in experiment
With triethylamine; In N,N-dimethyl-formamide;Reflux; A mixture of ethyl 2-(bromomethyl)-6-nitrobenzoate and H-CH2-CH3-Compound D, triethyl amine in DMF is heated to reflux. The solvent is removed in vacuo. The crude mixture is purified by column chromatography to give (S)-2-(1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-7-nitroisoindolin-1-one. A mixture of (S)-2-(1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)-7-nitroisoindolin-1-one and Pd/C in ethyl acetate is shaken under hydrogen. The suspension is filtered thru a pad of Celite. The solvent is removed in vacuo. The crude mixture is purified by column chromatography to give (S)-7-amino-2-(1-(3-ethoxy-4-methoxyphenyl)-2-(methylsulfonyl)ethyl)isoindolin-1-one.
 

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