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Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst

Received: 10 April 2015    Accepted: 22 April 2015    Published: 28 April 2015
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Abstract

In this method, at first the synthesis of 2,3-dihydro-1H-carbazol-4(9H)-one product by the condensation of (Z)-3-(2-phenylhydrazono)cyclohexanone in the presence of (SBA-Pr-SO3H) as nanoporous solid acid catalyst, acid acetic glacial and ethanol as solvent under reflux conditions is reported. (SBA-Pr-SO3H) nanoporous solid acid catalyst was used as an effective catalyst for the synthesis of Carvedilol from the reaction of 4-oxiranylmethyoxy-9H-carbazole and 2-(2-methoxyphenoxy)ethanamine in the presence of monoglyme solvent. This synthesis afforded under ring opening of 4-oxiranylmethyoxy-9H-carbazole with 2-(2-methoxyphenoxy)ethanamine by above nano-catalyst. Heterogeneous reaction conditions, easy procedure, short reaction time, and high yields are some important advantages of this method.

Published in American Journal of Heterocyclic Chemistry (Volume 1, Issue 1)
DOI 10.11648/j.ajhc.20150101.11
Page(s) 1-5
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Copyright

Copyright © The Author(s), 2024. Published by Science Publishing Group

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Keywords

Carvedilol, Nano-Catalyst, Carbazole, Heterogeneous, (SBA-Pr-SO3H), Synthesis

References
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    Ali Gharib, Nader Noroozi Pesyan, Leila Vojdani Fard, Mina Roshani. (2015). Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst. American Journal of Heterocyclic Chemistry, 1(1), 1-5. https://doi.org/10.11648/j.ajhc.20150101.11

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    ACS Style

    Ali Gharib; Nader Noroozi Pesyan; Leila Vojdani Fard; Mina Roshani. Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst. Am. J. Heterocycl. Chem. 2015, 1(1), 1-5. doi: 10.11648/j.ajhc.20150101.11

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    AMA Style

    Ali Gharib, Nader Noroozi Pesyan, Leila Vojdani Fard, Mina Roshani. Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst. Am J Heterocycl Chem. 2015;1(1):1-5. doi: 10.11648/j.ajhc.20150101.11

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  • @article{10.11648/j.ajhc.20150101.11,
      author = {Ali Gharib and Nader Noroozi Pesyan and Leila Vojdani Fard and Mina Roshani},
      title = {Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst},
      journal = {American Journal of Heterocyclic Chemistry},
      volume = {1},
      number = {1},
      pages = {1-5},
      doi = {10.11648/j.ajhc.20150101.11},
      url = {https://doi.org/10.11648/j.ajhc.20150101.11},
      eprint = {https://article.sciencepublishinggroup.com/pdf/10.11648.j.ajhc.20150101.11},
      abstract = {In this method, at first the synthesis of 2,3-dihydro-1H-carbazol-4(9H)-one product by the condensation of (Z)-3-(2-phenylhydrazono)cyclohexanone in the presence of (SBA-Pr-SO3H) as nanoporous solid acid catalyst, acid acetic glacial and ethanol as solvent under reflux conditions is reported. (SBA-Pr-SO3H) nanoporous solid acid catalyst was used as an effective catalyst for the synthesis of Carvedilol from the reaction of 4-oxiranylmethyoxy-9H-carbazole and 2-(2-methoxyphenoxy)ethanamine in the presence of monoglyme solvent. This synthesis afforded under ring opening of 4-oxiranylmethyoxy-9H-carbazole with 2-(2-methoxyphenoxy)ethanamine by above nano-catalyst. Heterogeneous reaction conditions, easy procedure, short reaction time, and high yields are some important advantages of this method.},
     year = {2015}
    }
    

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  • TY  - JOUR
    T1  - Synthesis of β-Receptor Blocker and Antihypertensive Drug Using (SBA-Pr-SO3H) as an Eco-Friendly, Inexpensive and Efficient Nano-Catalyst
    AU  - Ali Gharib
    AU  - Nader Noroozi Pesyan
    AU  - Leila Vojdani Fard
    AU  - Mina Roshani
    Y1  - 2015/04/28
    PY  - 2015
    N1  - https://doi.org/10.11648/j.ajhc.20150101.11
    DO  - 10.11648/j.ajhc.20150101.11
    T2  - American Journal of Heterocyclic Chemistry
    JF  - American Journal of Heterocyclic Chemistry
    JO  - American Journal of Heterocyclic Chemistry
    SP  - 1
    EP  - 5
    PB  - Science Publishing Group
    SN  - 2575-5722
    UR  - https://doi.org/10.11648/j.ajhc.20150101.11
    AB  - In this method, at first the synthesis of 2,3-dihydro-1H-carbazol-4(9H)-one product by the condensation of (Z)-3-(2-phenylhydrazono)cyclohexanone in the presence of (SBA-Pr-SO3H) as nanoporous solid acid catalyst, acid acetic glacial and ethanol as solvent under reflux conditions is reported. (SBA-Pr-SO3H) nanoporous solid acid catalyst was used as an effective catalyst for the synthesis of Carvedilol from the reaction of 4-oxiranylmethyoxy-9H-carbazole and 2-(2-methoxyphenoxy)ethanamine in the presence of monoglyme solvent. This synthesis afforded under ring opening of 4-oxiranylmethyoxy-9H-carbazole with 2-(2-methoxyphenoxy)ethanamine by above nano-catalyst. Heterogeneous reaction conditions, easy procedure, short reaction time, and high yields are some important advantages of this method.
    VL  - 1
    IS  - 1
    ER  - 

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Author Information
  • Department of Chemistry, Islamic Azad University, Mashhad, Iran

  • Department of Chemistry, Faculty of Science, Urmia University, Urmia, Iran

  • Education Ministry, Education Organization of Razavi Khorasan, Mashhad, Iran

  • Department of Chemistry, Islamic Azad University, Mashhad, Iran

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