1957
DOI: 10.1021/ja01568a039
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Pyridylethylated Benzoxazinediones1

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Cited by 24 publications
(8 citation statements)
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“…Methyl salicylate (3.3 mmol) and 3,4-dimethoxyphenethylamine (6.6 mmol) were mixed at room temperature under magnetic stirring for 6 hours to give 2-hydroxy-N-[2-(4-methoxyphenyl)ethyl]-benzamide (Rip-B, 34% yield). Melting point: 96 °C [23]. 1H and 13C-NMR date: see Table 1 and Table 2.…”
Section: Methodsmentioning
confidence: 99%
“…Methyl salicylate (3.3 mmol) and 3,4-dimethoxyphenethylamine (6.6 mmol) were mixed at room temperature under magnetic stirring for 6 hours to give 2-hydroxy-N-[2-(4-methoxyphenyl)ethyl]-benzamide (Rip-B, 34% yield). Melting point: 96 °C [23]. 1H and 13C-NMR date: see Table 1 and Table 2.…”
Section: Methodsmentioning
confidence: 99%
“…]ethyl-6-acyl-2-benzoxazolinones [22,23] To 0.1 mol 6-acyl-2-benzoxazolinone derivatives were added 8 ml 2-and/or 4-vinylpyridine and the reaction mixture heated under reflux in an oil bath until molten and then for 2 additional hours at 150°C. On cooling, the products were poured into crushed ice, and the solid mass which separated out was filtered, dried, and crystallized from ethanol.…”
Section: -[2-(2-/4-pyridyl)mentioning
confidence: 99%
“…On adding cold alcohol-water mixture, the product separated, the resulting precipitate was collected by filtration. The crude product was recrystallized from different solvents [22] .…”
Section: -[2-(2-/4-pyridyl)]ethyl-6-acyl-2-benzoxazolinone and 3-[2-mentioning
confidence: 99%