5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one

The title compound, 5-(1<i>H</i>-indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one, was synthesized for the first time by a one-step, two-component reaction between 1-methylbenzimidazole and benzoylindolyl-3-acetylene. The product was characterized by <sup&g...

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Main Authors: Kseniya V. Belyaeva, Denis N. Tomilin, Andrei V. Afonin, Boris A. Trofimov
Format: Article
Language:English
Published: MDPI AG 2022-10-01
Series:Molbank
Subjects:
Online Access:https://www.mdpi.com/1422-8599/2022/4/M1466
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author Kseniya V. Belyaeva
Denis N. Tomilin
Andrei V. Afonin
Boris A. Trofimov
author_facet Kseniya V. Belyaeva
Denis N. Tomilin
Andrei V. Afonin
Boris A. Trofimov
author_sort Kseniya V. Belyaeva
collection DOAJ
description The title compound, 5-(1<i>H</i>-indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one, was synthesized for the first time by a one-step, two-component reaction between 1-methylbenzimidazole and benzoylindolyl-3-acetylene. The product was characterized by <sup>1</sup>H-NMR, <sup>13</sup>C-NMR, IR spectroscopy and HRMS.
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spelling doaj.art-4a084c8eb5e741aba84b5733ed25ddd42023-11-24T16:53:46ZengMDPI AGMolbank1422-85992022-10-0120224M146610.3390/M14665-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-oneKseniya V. Belyaeva0Denis N. Tomilin1Andrei V. Afonin2Boris A. Trofimov3A.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Science, 664033 Irkutsk, RussiaA.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Science, 664033 Irkutsk, RussiaA.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Science, 664033 Irkutsk, RussiaA.E. Favorsky Irkutsk Institute of Chemistry, Siberian Branch, Russian Academy of Science, 664033 Irkutsk, RussiaThe title compound, 5-(1<i>H</i>-indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one, was synthesized for the first time by a one-step, two-component reaction between 1-methylbenzimidazole and benzoylindolyl-3-acetylene. The product was characterized by <sup>1</sup>H-NMR, <sup>13</sup>C-NMR, IR spectroscopy and HRMS.https://www.mdpi.com/1422-8599/2022/4/M1466nitrogen heterocycleselectron-deficient acetylenesdiazocinonesring-expansion
spellingShingle Kseniya V. Belyaeva
Denis N. Tomilin
Andrei V. Afonin
Boris A. Trofimov
5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one
Molbank
nitrogen heterocycles
electron-deficient acetylenes
diazocinones
ring-expansion
title 5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one
title_full 5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one
title_fullStr 5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one
title_full_unstemmed 5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one
title_short 5-(1<i>H</i>-Indol-3-yl)-1-methyl-3-phenyl-1,6-benzodiazocin-2(1<i>H</i>)-one
title_sort 5 1 i h i indol 3 yl 1 methyl 3 phenyl 1 6 benzodiazocin 2 1 i h i one
topic nitrogen heterocycles
electron-deficient acetylenes
diazocinones
ring-expansion
url https://www.mdpi.com/1422-8599/2022/4/M1466
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AT denisntomilin 51ihiindol3yl1methyl3phenyl16benzodiazocin21ihione
AT andreivafonin 51ihiindol3yl1methyl3phenyl16benzodiazocin21ihione
AT borisatrofimov 51ihiindol3yl1methyl3phenyl16benzodiazocin21ihione