An Efficient Synthesis of Novel Benzo-Fused Macrocyclic Dilactams

A facile synthetic approach was adopted towards the synthesis of benzo‐fused macrocyclic lactams 2a–2g via the base‐catalyzed condensation reaction of 2,2′‐[alkanediylbis(oxy)]bis[benzaldehydes] 3a–3c with N,N′‐substituted bis[2‐cyanoacetamide] derivatives 7a–7c (Scheme 2). The latter compounds were...

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Veröffentlicht in:Helvetica chimica acta 2013-07, Vol.96 (7), p.1290-1297
Hauptverfasser: Mekky, Ahmed E. M., Ahmed, Ahmed A. M., Elwahy, Ahmed H. M.
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Sprache:eng
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Zusammenfassung:A facile synthetic approach was adopted towards the synthesis of benzo‐fused macrocyclic lactams 2a–2g via the base‐catalyzed condensation reaction of 2,2′‐[alkanediylbis(oxy)]bis[benzaldehydes] 3a–3c with N,N′‐substituted bis[2‐cyanoacetamide] derivatives 7a–7c (Scheme 2). The latter compounds were obtained by the reaction of the appropriate diamines 6a–6c with ethyl 2‐cyanoacetate (4). Attempts to prepare the oxaaza macrocycles 2 by alternative pathways were also investigated. The novel pyrazolo‐fused macrocycles 13a and 13b were obtained in 48 and 52% yield, respectively, upon treatment of 2d and 2g with NH2NH2⋅H2O at 100° (Scheme 4).
ISSN:0018-019X
1522-2675
DOI:10.1002/hlca.201200529