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HRID 74456作成日:2026年10月26日

2-(ethoxycarbonyl)-1-tosyl-1H-indole-5-carboxylic acid → 1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl ester

https://huagongshe.com/reaction/74456

反応式

関与物質

役割名称HCID仕込み量
反応物2-(ethoxycarbonyl)-1-tosyl-1H-indole-5-carboxylic acidHCID 68004853—
溶媒WaterHCID 962—
溶媒Ethyl AcetateHCID 8857—
溶媒1,1-bis(1,1-dimethylethoxy)-N,N,N-trimethylamineHCID 547712—
生成物1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl esterHCID 68005321134.3%

反応条件

温度80 °C

反応手順

1-(Toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 2-ethyl ester (690 mg, 1.85 mmol) was dissolved in N,N-dimethylformamide di-tert-butyl acetal (3.0 ml), and stirred at 80° C. for two and half hours. N,N-dimethylformamide di-tert-butyl acetal (2.0 ml) was further added thereto and stirred at 80° C. for three hours. After cooling to room temperature, the reaction mixture was diluted with ethyl acetate (150 ml) and water (75 ml). The organic layer was isolated, washed with water and a saturated aqueous solution of sodium chloride, and then dried over anhydrous sodium sulfate. The desiccant was removed by filtration. The filtrate was concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography (hexane/ethyl acetate=25/1 to 5/1) to give 1-(toluene-4-sulfonyl)-1H-indole-2,5-dicarboxylic acid 5-tert-butyl ester 2-ethyl ester (551 mg, 69%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08829199B2
出典データセットuspto-grants-2014_09
ORD IDord-07437c96346649d795b3ab596e77bf25
出典メモuspto-grants-2014_09