Anodic oxidation of 3-amino-5-(pyrid-4-yl)-1, 2-dihydropyrid-2-one (amrinone)
✍ Scribed by Dr. V. Hagen; Dr. E. Klauschenz; Doz. Dr. F. Pragst
- Publisher
- John Wiley and Sons
- Year
- 1987
- Tongue
- English
- Weight
- 609 KB
- Volume
- 329
- Category
- Article
- ISSN
- 1615-4150
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
The molecular structure of the title radical compound, C 12 H 16 N 3 O 2 , has crystallographic C 2 symmetry. The dihedral angle between the pyridine and imidazole rings is 25.66 (15) .
Synthesis of 1‐Cyano‐4‐dimethylamino‐3‐(4‐pyridinyl)‐1,3‐butadiene‐1‐carboxylic Acid Derivatives and Their Cyclisation to 3‐Substituted 2‐Amino‐5‐(4‐pyridinyl)‐pyridines Including the Corresponding 1‐Oxides The vinylogous amidinium salt 1 is transformed to 1‐cyano‐4‐dimethylamino‐3‐(4‐pyridinyl)‐1,
In the title compound, C 18 H 22 NO 3 P, the molecules are linked by two N-HÁ Á ÁN hydrogen bonds to form sheets built from R 2 2 (8) rings.
In the title compound, C 24 H 25 Cl 2 N 2 O 3 P, the P atom adopts a distorted tetrahedral configuration. Weak intermolecular N-HÁ Á ÁN and C-HÁ Á ÁO hydrogen bonds are observed, and C-HÁ Á Á interactions also contribute to the crystal packing.