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N. D. Zelinsky Institute of Organic Chemistry Russian Academy of Sciences, 47 Leninsky Prospekt, 119991 Moscow, Russia
Nanotechnology Education and Research Center, South Ural State University, 76 Lenina Avenue, 454080 Chelyabinsk, Russia
Author to whom correspondence should be addressed.
Academic Editor: Fawaz Aldabbagh
Molbank 2021, 2021(3), M1248;
Received: 15 June 2021 / Revised: 22 June 2021 / Accepted: 24 June 2021 / Published: 5 July 2021
(This article belongs to the Special Issue Heterocycle Reactions)
New (2,3-dihydro-1H-indol-5-ylmethyl)amine was synthesized from 2-((1-acetylindolin-5-yl)methyl)isoindoline-1,3-dione by simultaneous deprotection of phthalimide and acetyl groups. The structure of the newly synthesized compounds was established by elemental analysis, high resolution mass-spectrometry, 1H, 13C NMR and IR spectroscopy and mass-spectrometry. The resulting compound is a convenient intermediate for various disubstituted 1-(indolin-5-yl)methanamines, which may be of interest as substances with useful pharmacological properties. View Full-Text
Keywords: 2,3-dihydroindoles (indolines); (2,3-dihydro-1H-indol-5-ylmethyl)amine; deprotection; biological activity 2,3-dihydroindoles (indolines); (2,3-dihydro-1H-indol-5-ylmethyl)amine; deprotection; biological activity
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MDPI and ACS Style

Ogurtsov, V.A.; Rakitin, O.A. (2,3-Dihydro-1H-indol-5-ylmethyl)amine. Molbank 2021, 2021, M1248.

AMA Style

Ogurtsov VA, Rakitin OA. (2,3-Dihydro-1H-indol-5-ylmethyl)amine. Molbank. 2021; 2021(3):M1248.

Chicago/Turabian Style

Ogurtsov, Vladimir A., and Oleg A. Rakitin 2021. "(2,3-Dihydro-1H-indol-5-ylmethyl)amine" Molbank 2021, no. 3: M1248.

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