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HRID 846596作成日:2026年10月26日

Methyl iodide → Methyl 1-methyl-1H-indazole-3-carboxylate

https://huagongshe.com/reaction/846596

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl iodideHCID 6328—
反応物Sodium hydrideHCID 24758—
反応物methyl 1H-indazole-3-carboxylateHCID 657476—
反応物HCID 178418361HCID 178418361—
溶媒DimethylformamideHCID 6228—
生成物Methyl 1-methyl-1H-indazole-3-carboxylateHCID 13900574—

反応条件

温度80 °C

反応手順

A solution of indazole-3-carboxylic acid methyl ester (2.76 g, 0.0159 mole) in dry dimethylformamide (20 ml) was added dropwise to a stirred suspension of 60% sodium hydride (oil dispersion) (0.67 g, 0.0176 mole) in dimethylformamide (50 ml). After the addition was completed and the evolution of the hydrogen ceased, the mixture was heated to 80° C. and then cooled to ambient temperature. A solution of methyl iodide (4.23 g, 0.030 mole) in dimethylformamide (10 ml) was added dropwise to the stirred reaction mixture. After stirring for 15 minutes, the mixture was warmed to 50° C. for 30 minutes, and then cooled to ambient temperature. The reaction mixture was diluted to a volume of 300 ml with ice/water and extracted with two 100 ml portions of methylene chloride. The extract was dried (magnesium sulfate), and concentrated to an oil. Dimethylformamide was distilled from the mixture and the residual oil was triturated with petroleum ether to obtain a solid. The solid (1.66 g, 55%) was collected by filtration and recrystallized from isooctane to give 1.20 g; mp 78°-79° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05137895
出典データセットuspto-grants-1992_08
ORD IDord-2a4b0acd3eb14b7c94eb24608747791b
出典メモuspto-grants-1992_08