2-Chloro-4,5-dihydroimidazole, Part X. Revisiting route to N-heteroarylimidazolidin-2-ones
✍ Scribed by Franciszek Sa̧czewski; Anita Bulakowska; Maria Gdaniec
- Publisher
- Journal of Heterocyclic Chemistry
- Year
- 2002
- Tongue
- English
- Weight
- 58 KB
- Volume
- 39
- Category
- Article
- ISSN
- 0022-152X
No coin nor oath required. For personal study only.
✦ Synopsis
Abstract
The ureidation reactions of 2‐ and 4‐picoline N‐oxides with 2‐chloro‐4,5‐dihydroimidazole are described. A mechanism of novel thioureidation reaction of 4‐picoline N‐oxide with 2‐(4,5‐dihydro‐1__H__‐imidazol‐2‐ylthioxy)‐4,5‐dihydro‐1__H__‐imidazole is proposed. Structural assignment is confirmed by ^1^H and ^13^C nmr as well as by X‐ray crystallography.
📜 SIMILAR VOLUMES
Lewis Acid Induced N-Methyleneamine Equivalents. Part 4. Addition of 2-Trimethylsilyloxyfuran to Catalytically Generated N-Methyleneamine Equivalents: Synthesis of 5-Aminomethyl-2,5dihydrofuran-2-ones. -Treatment of 1,3,5-hexahydrotriazines (I) or N-methoxymethylanilines ( IV) with catalytic Lewis