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Electrochemical synthesis of pyrido[1,2-a]pyrimidine derivatives. II. Electrochemical reduction of 2,6-dimethyl-3-ethyl-4-oxo-4H-pyrido[1,2-a]pyrimidine in aqueous media

✍ Scribed by E. Szebényi-Győry; V. Kovács-Mindler; I. Hermecz; B. Podányi; J. Brlik

Publisher
Springer
Year
1985
Tongue
English
Weight
466 KB
Volume
15
Category
Article
ISSN
0021-891X

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3-(2-Chloro­ethyl)-2-methyl-4-oxo-6,7,8,
3-(2-Chloro­ethyl)-2-methyl-4-oxo-6,7,8,9-tetra­hydro-4H-pyrido[1,2-a]pyrimidin-1-ium chloride
✍ Ravikumar, Krishnan ;Sridhar, Balasubramanian 📂 Article 📅 2006 🏛 International Union of Crystallography 🌐 English ⚖ 148 KB

In the title compound, C 11 H 16 ClN 2 O + ÁCl À , the chloroethyl side chain is in a synclinal conformation. The tetrahydropyridine ring adopts a half-chair conformation. The crystal structure is stabilized by intermolecular N-HÁ Á ÁCl hydrogen bonds.