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HRID 12307作成日:2026年10月24日

Bromine → 2-Bromo-6-methoxypyridin-3-amine

https://huagongshe.com/ja/reaction/12307

反応式

関与物質

役割名称HCID仕込み量
反応物BromineHCID 24408—
反応物Sodium ThiosulfateHCID 24477—
反応物6-Methoxy-3-pyridinylamineHCID 81121—
反応物Sodium AcetateHCID 517045—
溶媒Acetic AcidHCID 176—
生成物2-Bromo-6-methoxypyridin-3-amineHCID 15209324—

反応手順

A mixture of 1.83 g (14.7 mM) of 5-amino-2-methoxypyridine and 1.21 g (14.7 mM) of sodium acetate in 12 ml of acetic acid is prepared and 0.75 ml (14.7 mM) of bromine is added gently, with stirring and while maintaining at room temperature. The reaction mixture is kept stirring for 30 minutes, at room temperature, and 200 ml of saturated sodium thiosulfate solution are then added. The aqueous phase obtained is extracted twice with ethyl acetate. The combined organic phases are dried over magnesium sulfate and concentrated under reduced pressure. 3 g of the expected compound are obtained in the form of a violet-colored solid (quantitative yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07728002B2
出典データセットuspto-grants-2010_06
ORD IDord-27352282c0af4dfbb16addeee00b36b0
出典メモuspto-grants-2010_06