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HRID 1653634作成日:2026年10月27日

Sodium Iodide → methyl 3-[(4,6-dimethoxypyrimidin-2-yl)oxy]-6-(N-methyl-N-benzylamino)picolinate

https://huagongshe.com/reaction/1653634

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium IodideHCID 5238—
反応物DiisopropylethylamineHCID 81531—
反応物N-benzyl-N-methylcarbamoyl chlorideHCID 10464985—
反応物methyl 3-[(4,6-dimethoxypyrimidin-2-yl)oxy]picolinate N-oxideHCID 14425903—
溶媒AcetonitrileHCID 6342—
生成物methyl 3-[(4,6-dimethoxypyrimidin-2-yl)oxy]-6-(N-methyl-N-benzylamino)picolinateHCID 1523996932%

反応手順

20 g (77.1 mmol) of methyl 3-[(4,6-dimethoxypyrimidin-2-yl)oxy]picolinate N-oxide, 15 g (116 mmol) of diisopropylethylamine and 46.2 g (308.2 mmol) of sodium iodide were suspended in 200 ml of acetonitrile and stirred at room temperature for 15 minutes. To this mixture, 21.2 g (115.4 mmol) of N-methyl-N-benzylcarbamoyl chloride dissolved in 20 ml of acetonitrile was added at room temperature. The mixture was refluxed. Foaming started at a temperature slightly lower than the boiling point, and such foaming terminated in about 30 minutes. The reaction was continued for further 10 minutes. The reaction solution was poured into water and extracted with ethyl acetate. The extract was washed with water, dried, concentrated and then purified by silica gel column chromatography to obtain the desired product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05403816
出典データセットuspto-grants-1995_04
ORD IDord-cf59d4b1fa2d4d4481b66b5822abfd7e
出典メモuspto-grants-1995_04