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HRID 1161885作成日:2026年10月24日

Hydrogen Bromide → 4-Bromo-5-chloro-2-methyl-indole-1-carboxylic acid methyl ester

https://huagongshe.com/ja/reaction/1161885

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrogen BromideHCID 260—
反応物Sodium NitriteHCID 23668193—
反応物4-Amino-5-chloro-2-methyl-indole-1-carboxylic acid methyl esterHCID 66819957—
触媒copper(I) bromideHCID 24593—
溶媒WaterHCID 962—
溶媒Hydrobromide monohydrateHCID 22326455—
生成物4-Bromo-5-chloro-2-methyl-indole-1-carboxylic acid methyl esterHCID 66820113—

反応条件

温度0 °C

反応手順

4-Amino-5-chloro-2-methyl-indole-1-carboxylic acid methyl ester (2.04 g, 8.54 mmol) is suspended in a 4.8% solution of HBr in water (75 ml). After cooling to 0° C., a solution of sodium nitrite (1.23 g, 17.94 mmol) in water (30 ml) is slowly added during 20 minutes. After 30 minutes at 0° C., it is slowly added to a solution of copper(I) bromide (25.1 g, 175 mmol) in 48% HBr/H2O (75 ml), while the temperature is kept below 5° C. After the addition is complete, the suspension is stirred at RT for 2 hours and then at 85° C. for 5 minutes. After cooling to RT, the mixture is extracted with CH2Cl2/MeOH (95:5, 800 ml). The organic layer is washed with saturated aqueous NaCl solution, dried over Na2SO4 and concentrated. Purification by FCC (hexane/EtOAc 4:1) affords the title compound. 1H NMR (DMSO, 400 MHz) δ 2.61 (s, 3H), 4.03 (s, 3H), 6.56 (s, 3H), 7.46 (d, J=9 Hz, 1H), 8.05 (d, J=9 Hz, 1H); ES-MS: 303 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07820672B2
出典データセットuspto-grants-2010_10
ORD IDord-53f52f67c96149b7af108aea11d2cb73
出典メモuspto-grants-2010_10