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HRID 17161作成日:2026年10月24日

1H-Indole-2-carboxylic acid, 1-methyl- → 1-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-indole-2-carboxamide

https://huagongshe.com/ja/reaction/17161

反応式

関与物質

役割名称HCID仕込み量
反応物1H-Indole-2-carboxylic acid, 1-methyl-HCID 27695—
反応物Oxalyl chlorideHCID 65578—
反応物DiisopropylethylamineHCID 81531—
反応物4-(Tetramethyl-1,3,2-dioxaborolan-2-yl)anilineHCID 2734620—
触媒DimethylformamideHCID 6228—
溶媒DichloromethaneHCID 6344—
生成物1-methyl-N-(4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)phenyl)-1H-indole-2-carboxamideHCID 1845054370.2%

反応手順

A mixture of oxalyl chloride (0.35 mL) and dimethylformamide (1 drop) was added to a solution of 1-methyl-1H-2-indolecarboxylic acid (440 mg, 2.51 mmol) in dichloromethane (10 mL). After one hour the mixture was evaporated, dissolved in dichloromethane (10 mL), and added to a mixture of 4-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)aniline (500 mg, 2.28 mmol) and diisopropylethylamine (0.35 mL) in dichloromethane (10 mL). After 16 hours the mixture was washed with water (10 mL), dried (MgSO4), filtered, concentrated, and purified by flash column chromatography to provide the desired product (600 mg, 1.60 mmol) after lyophilization: MS m/e 377.4 (M+H)+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07737160B2
出典データセットuspto-grants-2010_06
ORD IDord-00dd9d9dddeb4439adc214beea6eb3c3
出典メモuspto-grants-2010_06