Advertisement

Springer Nature is making SARS-CoV-2 and COVID-19 research free. View research | View latest news | Sign up for updates

Synthese von Thieno[2,3—f]chinolin-Derivaten

Synthesis of thieno[2.3—f]quinolines

Abstract

Catalytic hydrogenation of 2.3-dihydro-thieno[2.3−f]-quinoline-1.1-dioxide yielded 2.3.6.7.8.9-hexahydrothieno-[2.3−f]quinoline-1.1-dioxide, which was substituted via the corresponding chloroacyl compounds to several 6-aminoacyl-derivatives.Skraup's synthesis using 6-amino-2.3-dihydro-3-morpholino-benzo[b]thiophen-1.1-dioxide gave 2.3-dihydro-3-morpholino-thieno[2.3−f]quinoline.

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

Literature

  1. 1

    F. Sauter, Mh. Chem.99, 1591 (1968).

  2. 2

    F. Challenger undH. Clapham, J. chem. Soc. [London]1948, 1615.

  3. 3

    F. Sauter, Österr. Pat. Nr. 315 179 (28. 1. 1974; Anmeldung: 29. 3. 1972).

Download references

Author information

Rights and permissions

Reprints and Permissions

About this article

Cite this article

Sauter, F., Büyük, G. Synthese von Thieno[2,3—f]chinolin-Derivaten. Monatshefte für Chemie 105, 877–881 (1974). https://doi.org/10.1007/BF00912988

Download citation