Synthesis of N,N′-di(1-adamantyl)bispidin-9-ones
- Авторы: Kuznetsov A.I.1, Senan I.M.1,2, Alasadi R.T.1,3, Abdulnabi N.M.1,4, Serova T.M.5
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Учреждения:
- Moscow Technological University
- University of Sana
- University of Kerbala
- University of Al-Mustansiria
- Institute of Physiologically Active Compounds, Russian Academy of Sciences
- Выпуск: Том 67, № 6 (2018)
- Страницы: 1110-1113
- Раздел: Brief Communications
- URL: https://bakhtiniada.ru/1066-5285/article/view/242657
- DOI: https://doi.org/10.1007/s11172-018-2189-1
- ID: 242657
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Аннотация
The condensation product of adamantan-1-amine with formaldehyde, 1,3,5-tri(1-adamantyl)-1,3,5-triazacyclohexane, was treated with three different types of ketones: symmetric (RCH2)2CO, nonsymmetric RCH2COCH3, and acetone to obtain 1,5-R-N,N′-di(1-adamantyl) bispidin-9-ones, N,N′-di(1-adamantyl)-1-[(1-adamantylamino)methyl]-5-methylbispidin-9-one, and N,N′-di(1-adamantyl)-1,5-bis[(1-adamantylamino)methyl]bispidin-9-one. 1,5-R-N,N′-Di(1-adamantyl)bispidin-9-ones were reduced with sodium borohydride to 1,5-R-N,N′-di(1-adamantyl)bispidin-9-ols.
Об авторах
A. Kuznetsov
Moscow Technological University
Автор, ответственный за переписку.
Email: tetraza@mail.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571
I. Senan
Moscow Technological University; University of Sana
Email: tetraza@mail.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571; Sana
R. Alasadi
Moscow Technological University; University of Kerbala
Email: tetraza@mail.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571; Kerbala
N. Abdulnabi
Moscow Technological University; University of Al-Mustansiria
Email: tetraza@mail.ru
Россия, 86 prosp. Vernadskogo, Moscow, 119571; Baghdad
T. Serova
Institute of Physiologically Active Compounds, Russian Academy of Sciences
Email: tetraza@mail.ru
Россия, 1 Severnyi pr-d, Chernogolovka, Moscow Region, 142432
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