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HRID 1599341作成日:2026年10月25日

Ethanol → 2-Methylamino3-nitro-6-phenylpyridine

https://huagongshe.com/reaction/1599341

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 1048957577.7%

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 4.75 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US05739345
出典データセットuspto-grants-1998_04
ORD IDord-d0b4812a49ae46a3a5fb3b14fc6ae401
出典メモuspto-grants-1998_04