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Regioselective Reaction of N1-Benzyl-N2-(4-nitrophenyl)ethanediamide and Acetylenic Esters

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Summary.

The regioselective reaction of N1-benzyl-N2-(4-nitrophenyl)ethanediamide with dialkyl acetylenedicarboxylates or alkyl propiolates in the presence of triphenylphosphine leads to dialkyl 4-benzylamino-1-(4-nitrophenyl)-5-oxo-2,5-dihydro-1H-pyrrole-2,3-dicarboxylates or alkyl 4-benzylamino-1-(4-nitrophenyl)-2-oxo-5-pyrrolidinecarboxylates in good yields.

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Authors and Affiliations

  1. Department of Chemistry, Tarbiat Modarres University, P.O. Box 14115-175, Tehran, Iran

    Issa Yavari, Loghman Moradi, Farough Nasiri & Hoorieh Djahaniani

Authors
  1. Issa Yavari
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  2. Loghman Moradi
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  3. Farough Nasiri
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  4. Hoorieh Djahaniani
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Correspondence to Issa Yavari.

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Yavari, I., Moradi, L., Nasiri, F. et al. Regioselective Reaction of N1-Benzyl-N2-(4-nitrophenyl)ethanediamide and Acetylenic Esters. Monatsh. Chem. 136, 1757–1761 (2005). https://doi.org/10.1007/s00706-005-0367-y

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  • DOI: https://doi.org/10.1007/s00706-005-0367-y

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