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.
Ring transformation of 4-oxo-1,6,7,8-tetrahydro-4H-pyrido[1,2-a]-pyrimidine-3-carboxamide
✍ Scribed by István Hermecz; József Engler; Zoltán Mészáros; Gábor Tóth
- Publisher
- Elsevier Science
- Year
- 1979
- Tongue
- French
- Weight
- 145 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0040-4039
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