Skip to main content
Log in

Substituted pyridines

5-Methyl-4-phenyl-2-(aminoalkoxy, aroxymethyl)pyridines

  • Published:
Chemistry of Heterocyclic Compounds Aims and scope

Abstract

5-Methyl-4-phenyl-2-bromomethylpyridine, obtained from 2,5-dimethyl-4-phenylpyridine via the Wohl-Ziegler reaction, was used in the syntheses of substituted 2-aminomethyl-, 2-ethoxymethyl-, and 2-phenoxymethylpyridines.

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. N. S. Prostakov and N. N. Mikheeva, Med. Prom., No. 2, 11 (1960).

    Google Scholar 

  2. M. Hasegawa, Chem. Pharm. Bull. (Tokyo), 1, 293 (1953).

    Google Scholar 

  3. B. H. Walker, J. Org. Chem., 25, 1047 (1960).

    Google Scholar 

Download references

Author information

Authors and Affiliations

Authors

Additional information

Translated from Khimiya Geterotsiklicheskikh Soedinenii, No. 9, pp. 1211–1212, September, 1971.

Rights and permissions

Reprints and permissions

About this article

Cite this article

Prostakov, N.S., Baktibaev, O.B. Substituted pyridines. Chem Heterocycl Compd 7, 1137–1138 (1971). https://doi.org/10.1007/BF00510021

Download citation

  • Received:

  • Issue Date:

  • DOI: https://doi.org/10.1007/BF00510021

Keywords

Navigation