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HRID 42521作成日:2026年10月26日

Hydrochloric Acid → 3-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acid

https://huagongshe.com/reaction/42521

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物MethanolHCID 887—
反応物Sodium MethoxideHCID 10942334—
反応物methyl 6-bromo-1-isopropyl-3-methyl-1H-indole-4-carboxylateHCID 67464634—
触媒Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒N-methyl-2-pyrrolidoneHCID 13387—
生成物3-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acidHCID 6746533180%

反応条件

温度120 °C

反応手順

To methyl 6-bromo-3-methyl-1-(1-methylethyl)-1H-indole-4-carboxylate (1.3 g, 4.19 mmol) and copper(I) iodide (1.0 g, 5.25 mmol) was added NMP (8 mL). To the mixture was added dropwise a solution of sodium methoxide 25 wt % in methanol (4.0 mL, 17.49 mmol) with stirring. The reaction was heated to 120° C. and stirred for 1.5 hr. The reaction was allowed to cool and when the temperature reached 80° C., water (200 uL) was added. The reaction was allowed to continue to cool to RT and stirred overnight. The reaction was acidified with 1 N HCl (17 mL) and diluted with water and EtOAc. The mixture was filtered through Celite and washed with EtOAc. The filtrate was poured into a reparatory funnel and the organic phase was separated, washed with brine, dried (MgSO4), filtered, and concentrated under vacuum. Purification by silica gel chromatography (Analogix, SF25-60 g, 20 to 50% EtOAc in hexanes) gave after concentration, trituration with hexanes, filtration and drying under vacuum 3-methyl-1-(1-methylethyl)-6-(methyloxy)-1H-indole-4-carboxylic acid (825 mg, 3.34 mmol, 80% yield) as an light yellow solid. MS (ES)+m/e 248.3 [M+H]+.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08536179B2
出典データセットuspto-grants-2013_09
ORD IDord-3a4122d414294dfaaf613ffb1bed093d
出典メモuspto-grants-2013_09