Synthesis of Pyrimido[6,1-a]isoquinolines by the Reaction of Thriethyl Orthoformate with Enamines of 3,3-dialkyl-1,2,3,4-tetrahydroisoquinoline series
- Authors: Mikhailovskii A.G.1, Peretyagin D.A.1
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Affiliations:
- Perm State Pharmaceutical Academy
- Issue: Vol 55, No 5 (2019)
- Pages: 721-723
- Section: Short Communications
- URL: https://journal-vniispk.ru/1070-4280/article/view/220665
- DOI: https://doi.org/10.1134/S1070428019050233
- ID: 220665
Cite item
Abstract
Boiling (Z)-2-[3,3-dimethyl-3,4-dihydroisoquinolin-1(2H)-ylidene]acetamides in AcOEt/Ac2O leads involves annelation of the pyrimidine ring to form 6,6-dimethyl-6,7-dihydro-2H-pyrimido[6,1-a]-isoquinolin-2-ones. Similarly, benzo[f]isoquinoline amides form in this reaction 12,12-dialkyl-11,12-dihydro-3H-benzo[f]pyrimido[6,1-a]isoquinolin-3-ones.
About the authors
A. G. Mikhailovskii
Perm State Pharmaceutical Academy
Author for correspondence.
Email: neorghim@pfa.ru
Russian Federation, ul. Polevaya 2, Perm, 614990
D. A. Peretyagin
Perm State Pharmaceutical Academy
Email: neorghim@pfa.ru
Russian Federation, ul. Polevaya 2, Perm, 614990
Supplementary files
