Reaction of 3-aminoquinoline-2,4-diones with nitrourea. Synthetic route to novel 3-ureidoquinoline-2,4-diones and imidazo[4,5-c]quinoline-2,4-diones
✍ Scribed by Antonín Klásek; Antonín Lyčka; Michal Holčapek; Ignác Hoza
- Book ID
- 108282738
- Publisher
- Elsevier Science
- Year
- 2004
- Tongue
- French
- Weight
- 179 KB
- Volume
- 60
- Category
- Article
- ISSN
- 0040-4020
No coin nor oath required. For personal study only.
📜 SIMILAR VOLUMES
## Abstract magnified image 3‐Alkyl/aryl‐3‐amino‐1__H__,3__H__‐quinoline‐2,4‐diones react with alkyl/aryl isocyanates to give novel 3‐alkyl/aryl‐3‐ureido‐1__H__,3__H__‐quinoline‐2,4‐diones or 3a‐alkyl/aryl‐9b‐hydroxy‐3,3a,5,9b‐tetrahydro‐1__H__‐imidazo[4,5‐__c__]quinoline‐2,4‐diones. In some cases
Reaction of 1-alkyl/aryl-3-amino-1H,3H-quinoline-2,4-diones with urea. Synthetic route to novel 3-(3-acylureido)
## Abstract The preparation of 2,3a,4,5‐tetrahydrofuro[2,3‐__c__]quinoline‐2,4‐diones starting from 3‐hydroxy‐1,2,3,4‐tetrahydroquinoline‐2,4‐diones and using the reaction path __via__ bromoacetylderivatives and triphenylphosphonioacetyl derivatives of the initial substances is described. The nmr s