Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst

Abstract A one-pot three component reaction of benzaldehydes, 1H-tetrazole-5-amine, and 3-cyanoacetyl indole in the presence of a new hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework as a recyclable catalyst was explored. This novel catalyst, which was fully characterize...

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Autores principales: Mohammad Hossein Abdollahi-Basir, Boshra Mirhosseini-Eshkevari, Farzad Zamani, Mohammad Ali Ghasemzadeh
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Publicado: Nature Portfolio 2021
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Acceso en línea:https://doaj.org/article/594cf8572fa9484fbc0b9e3359d41274
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spelling oai:doaj.org-article:594cf8572fa9484fbc0b9e3359d412742021-12-02T13:30:51ZSynthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst10.1038/s41598-021-84379-32045-2322https://doaj.org/article/594cf8572fa9484fbc0b9e3359d412742021-03-01T00:00:00Zhttps://doi.org/10.1038/s41598-021-84379-3https://doaj.org/toc/2045-2322Abstract A one-pot three component reaction of benzaldehydes, 1H-tetrazole-5-amine, and 3-cyanoacetyl indole in the presence of a new hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework as a recyclable catalyst was explored. This novel catalyst, which was fully characterized by XRD, FE-SEM, EDX, FT-IR, TGA, BET, and TEM exhibited outstanding catalytic activity for the preparation of a range of pharmaceutically important tetrazolo[1,5-a]pyrimidine-6-carbonitriles with good to excellent yields in short reaction time.Mohammad Hossein Abdollahi-BasirBoshra Mirhosseini-EshkevariFarzad ZamaniMohammad Ali GhasemzadehNature PortfolioarticleMedicineRScienceQENScientific Reports, Vol 11, Iss 1, Pp 1-12 (2021)
institution DOAJ
collection DOAJ
language EN
topic Medicine
R
Science
Q
spellingShingle Medicine
R
Science
Q
Mohammad Hossein Abdollahi-Basir
Boshra Mirhosseini-Eshkevari
Farzad Zamani
Mohammad Ali Ghasemzadeh
Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst
description Abstract A one-pot three component reaction of benzaldehydes, 1H-tetrazole-5-amine, and 3-cyanoacetyl indole in the presence of a new hexamethylenetetramine-based ionic liquid/MIL-101(Cr) metal–organic framework as a recyclable catalyst was explored. This novel catalyst, which was fully characterized by XRD, FE-SEM, EDX, FT-IR, TGA, BET, and TEM exhibited outstanding catalytic activity for the preparation of a range of pharmaceutically important tetrazolo[1,5-a]pyrimidine-6-carbonitriles with good to excellent yields in short reaction time.
format article
author Mohammad Hossein Abdollahi-Basir
Boshra Mirhosseini-Eshkevari
Farzad Zamani
Mohammad Ali Ghasemzadeh
author_facet Mohammad Hossein Abdollahi-Basir
Boshra Mirhosseini-Eshkevari
Farzad Zamani
Mohammad Ali Ghasemzadeh
author_sort Mohammad Hossein Abdollahi-Basir
title Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst
title_short Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst
title_full Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst
title_fullStr Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst
title_full_unstemmed Synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using HMTA-BAIL@MIL-101(Cr) as a superior heterogeneous catalyst
title_sort synthesis of tetrazolo[1,5-a]pyrimidine-6-carbonitriles using hmta-bail@mil-101(cr) as a superior heterogeneous catalyst
publisher Nature Portfolio
publishDate 2021
url https://doaj.org/article/594cf8572fa9484fbc0b9e3359d41274
work_keys_str_mv AT mohammadhosseinabdollahibasir synthesisoftetrazolo15apyrimidine6carbonitrilesusinghmtabailmil101crasasuperiorheterogeneouscatalyst
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