1,5-Dimethyl-2-nitrimino-1,2-dihydropyridine
✍ Scribed by Kyzioł, Janusz B. ;Nogły, Przemysław ;Daszkiewicz, Zdzisław ;Zaleski, Jacek
- Publisher
- International Union of Crystallography
- Year
- 2006
- Tongue
- English
- Weight
- 264 KB
- Volume
- 62
- Category
- Article
- ISSN
- 1600-5368
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✦ Synopsis
Methylation of 5-methyl-2-nitraminopyridine provides the title compound, C 7 H 9 N 3 O 2 , as the only product. The molecule consists of two planar fragments, viz. an aromatic ring and a nitrimino substituent. The NNO 2 group is twisted by 17 (2) out of the plane of the pyridine ring. Despite a small torsion angle between these fragments, the geometry of the molecule indicates the participation of the -electrons in the C-N bond. The hydrogen bonds in the crystal structure seem to be too weak to generate any deformations observed in the molecule.
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## Abstract On irradiation (350 nm) in the presence of excess 2,3‐dimethylbut‐2‐ene, the newly synthesized title compound 5 affords as main products the unexpected cyclopropylpyrrolidine 10 (50%) and the spiro‐oxetane 9 (25%).