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A facile and efficient route to one-pot synthesis of new cyclophanes using vinamidinium salts.

ABSTRACT: In this study, an efficient method for the synthesis of new cyclophanes (5a-f, 6a-g) through the condensation of 1,4-phenylenedimethanamine (3) or 2,3,5,6-tetramethylbenzene-1,4-diamine (4) with 2-substituted vinamidiniums (2a-g) is described. The cyclophane derivatives are obtained in good to excellent yields in the presence of acetic acid in refluxing acetonitrile after 15 h. The structure of new compounds was validated based on their spectral data (¹H NMR, ¹³C NMR, IR) and elemental analysis.

SUBMITTER: Golzar N

PROVIDER: S-EPMC8697689 | biostudies-literature | 2021 Apr

REPOSITORIES: biostudies-literature

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A facile and efficient route to one-pot synthesis of new cyclophanes using vinamidinium salts.

Golzar Nooshin N Mehranpour Abdolmohammad A Nowrouzi Najmeh N

RSC advances 20210413 22

In this study, an efficient method for the synthesis of new cyclophanes (5a-f, 6a-g) through the condensation of 1,4-phenylenedimethanamine (3) or 2,3,5,6-tetramethylbenzene-1,4-diamine (4) with 2-substituted vinamidiniums (2a-g) is described. The cyclophane derivatives are obtained in good to excellent yields in the presence of acetic acid in refluxing acetonitrile after 15 h. The structure of new compounds was validated based on their spectral data (1H NMR, 13C NMR, IR) a ...[more]

PMID: 35423896

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