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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This is an Open Access article, distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution and reproduction in any medium or format, provided the original work is properly cited. |
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Copyright © The Author(s), 2015. Published by Science Publishing Group |
Carvedilol, Nano-Catalyst, Carbazole, Heterogeneous, (SBA-Pr-SO3H), Synthesis
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APA Style
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
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
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
@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} }
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 -