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HRID 55541作成日:2026年10月25日

Ethanol → 2-Methylamino3-nitro-6-phenylpyridine

https://huagongshe.com/reaction/55541

反応式

関与物質

役割名称HCID仕込み量
反応物EthanolHCID 702—
反応物Sodium CarbonateHCID 10340—
反応物6-chloro-N-methyl-3-nitropyridin-2-amineHCID 10750094—
反応物PhenylborateHCID 19793864—
触媒Palladium hydroxideHCID 9942167—
溶媒TolueneHCID 1140—
生成物2-Methylamino3-nitro-6-phenylpyridineHCID 104895757,773.9%

反応条件

温度105 °C

反応手順

50 ml of a 2N aqueous solution of sodium carbonate and 0.34 g of 20% w/w palladium hydroxide on charcoal were added to a solution of 5.0 g of 6-chloro-2-methylamino-3-nitropyridine (prepared as described in Preparation 66) and 3.9 g of phenyl borate in 80 ml of a 1:1 by volume mixture of ethanol and toluene, and the resulting mixture was stirred at 105° C. for 4.5 hours. At the end of this time, the reaction mixture was filtered to remove the palladium hydroxide on charcoal. The filtrate was concentrated by evaporation under reduced pressure, and the concentrate was diluted with water, after which it was extracted with ethyl acetate. The extract was washed with water and dried over anhydrous sodium sulfate, after which the solvent was removed by distillation under reduced pressure. The residue was crystallized by trituration with ethanol, to give 475 g of the title compound, melting at 98°-99° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05624935
出典データセットuspto-grants-1997_04
ORD IDord-3d62ed38c2974e79a7fb0852201ac7ad
出典メモuspto-grants-1997_04