Synthesis of 6-Substituted-3-hydroxy-4(1H)-pyridinones: Oxidation-Michael Addition of 3-Hydroxy-4(1H)-pyridinones. -The oxidation of pyridinones of type (I) with Ag 2 O involving alcohols (II) is reported for the first time. The resulting pyridinediones subsequently undergo Michael addition with thi
Synthesis of new substituted 1-(3-pyridyl)pyridinium salts and 3,4-diamino-2(1H)-pyridinones
✍ Scribed by Gewald, Karl ;Rehwald, Matthias ;Müller, Heike ;Bellmann, Peter
- Publisher
- John Wiley and Sons
- Year
- 1995
- Tongue
- English
- Weight
- 456 KB
- Volume
- 1995
- Category
- Article
- ISSN
- 0947-3440
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✦ Synopsis
Pyridines
2-[ (Chloroacetyl)amino]acrylonitriles 1 and 3-[ (chloroacety1)-ridinones 8. Analogously to other orfho-diamines, the substi-
(1.92 g, 20 mmol) and dry K2C03 (4.2 g, 30 mmol) in dioxane (15 ml) were stirred at 6 0 T , and chloroacetyl chloride (3.4 g, 30 mmol) was added dropwise within 1 h to the reaction mixture. After additional stirring at 60°C for 1 h and cooling to room temp. the reaction mixture was poured into water (100 ml). Filtration and washing with water afforded crude l a (2.2 g, 58%), m.p. 51-54°C (benzene). -C7H9C1N20 .
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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.
## Abstract magnified image Several 4‐substituted‐3, 5‐bis(2‐pyridyl)‐1__H__‐pyrazoles, where the substituent is chloro, bromo, iodo, nitro, diazo, were synthesized under mild reaction conditions in high yields. The structures of the products were characterized by ^1^H NMR, ^13^C NMR, ESI‐MS, IR a
## 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.