## Abstract The cyclization of phenacyl anthranilate has been studied with the aim to develop the synthesis of 2‐(2′‐aminophenyl)‐4‐phenyloxazole. However, a different course of the reaction than expected was observed. 2‐Phenyl‐2‐hydroxymethyl‐4‐oxo‐1,2,3,4‐tetrahydroquinazoline (**3a**) was formed
Formation of 4,4-Dialkyl-2-oxo-morpholinium Chlorides. II
✍ Scribed by Prof. Dr. Stanisław Witek; Dr. Małgorzata Os̀wieşcimska
- Publisher
- John Wiley and Sons
- Year
- 1980
- Tongue
- English
- Weight
- 471 KB
- Volume
- 322
- Category
- Article
- ISSN
- 1615-4150
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✦ Synopsis
Zur Bildung von 4,4‐Dialkyl‐2‐oxo‐morpholinium‐chloriden
Dialkylaminoethanole 2 reagieren mit Chloracetaten 1 zu den N,N‐Dialkyl‐2‐oxo‐morpholinium‐salzen 6. Es wird gezeigt, daß die Reaktion zweistufig und über die Ester 3–5 verläuft, welche zu den Salzen 6 cyclisieren. Das Zwischenprodukt 5a wurde isoliert, seine Struktur aufgeklärt und ein Reaktionsmechanismus vorgeschlagen.
2‐Oxo‐morpholiniumsalze 6 hydrolysieren in wäßriger Lösung zu den entsprechenden Betainen 7. Der Hydrolysegrad wurde bestimmt. Die Betaine 7 können in umgekehrter Weise zu den 2‐Oxomorpholinium‐Derivaten 6 cyclisieren.
📜 SIMILAR VOLUMES
Our study demonstrated that 4-(4,6-dimethoxy-1,3,5-triazine-2-yl)-4-methyl-morpholinium chloride (DMTMM) is a versatile coupling reagent for the synthesis of sterically-hindered peptidomimetics. It is superior to HBTU/HOBt and CDMT in controlling racemization and N-arylation, respectively.
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## Abstract ChemInform is a weekly Abstracting Service, delivering concise information at a glance that was extracted from about 200 leading journals. To access a ChemInform Abstract, please click on HTML or PDF.