A convenient synthesis of trifluoroacetamide derivatives of diaza[3 2]cyclophanes and triaza[33]cyclophanes

Hideki Okamoto, Hiroyuki Takemura, Kyosuke Satake

Research output: Contribution to journalArticlepeer-review

5 Citations (Scopus)


The diaza[32]cyclophane skeleton has been constructed by the bis-N-alkylation of 1,4-bis[(4-nitrophenylsulfonylamino)methyl]benzene with 1,4-bis(halomethyl)benzene in the presence of sodium hydride. The 4-nitrophenylsulfonyl (Ns) amides in the bridge chains of the cyclophane were effectively deprotected by sodium ethanethiolate and the resulting free amine moieties were reprotected as the trifluoroacetamide under mild conditions to afford 3,7-bis(trifluoroacetyl)-3,7-diaza-1,5(1,4)-dibenzenacyclooctaphane in 26% overall yield. This Ns-amide method has also been applied for the preparation of a higher homologue, the trifluoroacetamide derivative of triaza[33]cyclophane, 3,5,7-tris(trifluoroacetyl)-3,7,10-triaza-1, 5(1,3,5)-dibenzenabicyclo[3.3.3]undecaphane, in 18% overall yield. Thus, the present procedure provides a convenient synthetic route to azacyclophane derivatives possessing trifluoroacetamide groups in the bridge chains.

Original languageEnglish
Pages (from-to)39-44
Number of pages6
Issue number1
Publication statusPublished - Jan 3 2008


  • Amides
  • Amines
  • Chromophores
  • Cyclophanes
  • Sulfonamides

ASJC Scopus subject areas

  • Catalysis
  • Organic Chemistry


Dive into the research topics of 'A convenient synthesis of trifluoroacetamide derivatives of diaza[3 2]cyclophanes and triaza[33]cyclophanes'. Together they form a unique fingerprint.

Cite this