4,5-dihydroisoxazoles, IX. Reactions of 3-aryl-4,5-dihydro-4-methylene-5-morpholinoisoxazoles with 2,4-diaryl-5(4H)-oxazolones: A new synthesis of tetrahydro-6-oxo-3-pyridinecarbaldehydes
✍ Scribed by Erba, Emanuela ;Pocar, Donato
- Publisher
- John Wiley and Sons
- Year
- 1990
- Tongue
- English
- Weight
- 277 KB
- Volume
- 1990
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Abstract
The 5(4__H__)‐oxazolones 1a–e react with 5‐morpholinoisoxazoles 2a–b to afford the 4‐[(4‐isoxazolyl)methyl]‐5(4__H__)‐oxazolones 3a–g. Compounds 3 are hydrogenated with Pd/C in dioxane to yield the corresponding 1,4,5,6‐tetrahydro‐6‐oxo‐3‐pyridinecarbaldehydes 6a–d.
📜 SIMILAR VOLUMES
## Abstract Several new 6‐amino‐ and 6,8‐diamino‐4‐aryl‐2,3‐dihydropyrimido[4,5‐__b__][1,4]diazepines were obtained from the reaction of 4,5,6‐triaminopyrimidine **1a** and 2,4,5,6‐tetraaminopyrimidine **1b** with one equivalent of 3‐dimethylaminopropiophenones **2** in absolute ethanol. Structure
## Abstract A series of 3a,5‐diaryl‐1,3‐diphenyl‐3a,4,5,6‐tetrahydro‐3H‐1,2,4‐triazolo[4,3‐a][1,5]benzo‐diazepines was synthesized by the cycloaddition reactions of 2,4‐diaryl‐2,3‐dihydro‐1H‐1,5‐benzo‐diazepines and N‐phenylbenzonitrileimine generated from N‐phenylbenzenecarbohydrazonic chloride in