Skip to main content
Log in

4-Trifluoroacetamidobenzotriazole N2-2,3,4-tri-O-acetyl-β-D-ribopyranoside

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

4-Trifluoroacetamidobenzotriazole (I) was synthesized by acylation of 4-aminobenzotriazole with trifluoroacetic anhydride under mild conditions in pyridine. The silver salt (II) of I was obtained by treatment of base I with an aqueous alcohol solution of AgNO3. Condensation of silver salt II with 1-bromo-2,3,4-tri-O-acetyl-D-ribopyranoside leads to 4-trifluoroacetamidobenzotriazole N2-2,3,4-tri-O-acetyl-β-D-ribopyranoside (III). The structure of nucleoside III was confirmed by its IR, UV, and PMR spectra.

This is a preview of subscription content, log in via an institution to check access.

Access this article

Price excludes VAT (USA)
Tax calculation will be finalised during checkout.

Instant access to the full article PDF.

Similar content being viewed by others

Literature cited

  1. V. P. Chernetskii, É. E. Rengevich, L. S. Usenko, and I. F. Franchuk, Khim. Geterotsikl. Soedin., No. 10, 1429 (1971).

    Google Scholar 

  2. E. E. Rengevich, V. P. Chernetskii, and L. S. Usenko, Ukr. Khim. Zh., 41, 635 (1975).

    Google Scholar 

  3. L. Bellamy, Infrared Spectra of Complex Molecules, Methuen (1958).

  4. D. Monte, A. Mangini, R. Passarini, and C. Gauti, Gazz. Chim. Ital., 88, 977 (1958).

    Google Scholar 

  5. G. T. Roger, and T. L. V. Vibricht, Tetrahedron Lett., No. 2, 1025 (1968).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 12, pp. 1691–1692, December, 1978.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Kul'chitskii, M.M., Bogacheva, S.V. 4-Trifluoroacetamidobenzotriazole N2-2,3,4-tri-O-acetyl-β-D-ribopyranoside. Chem Heterocycl Compd 14, 1375–1377 (1978). https://doi.org/10.1007/BF00487412

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00487412

Keywords

Navigation