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HRID 1054662作成日:2026年10月25日

Water → methyl 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1054662

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物Potassium CarbonateHCID 11430—
反応物Benzene, 4-bromo-1,2-dimethoxy-HCID 76114—
反応物methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylateHCID 86698665—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒EthanolHCID 702—
溶媒TolueneHCID 1140—
溶媒Ethyl AcetateHCID 8857—
生成物methyl 6-chloro-5-(3,4-dimethoxyphenyl)-1H-indole-3-carboxylateHCID 8669866684%

反応条件

温度110 °C

反応手順

A mixture of methyl 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole-3-carboxylate (100 mg, 0.31 mmol), 4-bromoveratrole (83 mg, 0.37 mmol), and aqueous potassium carbonate solution (2 M, 0.62 mL, 1.24 mmol) in toluene (1.8 mL) and ethanol (0.6 mL) was degassed with nitrogen for 5 minutes then treated with [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium(II) (13.8 mg, 0.016 mmol). The reaction mixture was heated to 110° C. for 2.5 h. The reaction was cooled to room temperature and poured into water and ethyl acetate. The layers were separated and the aqueous layer was back-extracted twice with ethyl acetate. The combined organic layers were dried over sodium sulfate, filtered, and concentrated in vacuo. Flash column chromatography was performed on the crude product using heptanes/ethyl acetate (4:1 to 1:1) to give the title compound (90 mg 84%). MS (ES+) 346.2 (M+H)+. 1H NMR (500 MHz, DMSO-d6) δ 12.05 (br. s., 1 H), 8.17 (s, 1 H), 7.94 (s, 1 H), 7.64 (s, 1 H), 7.04 (d, J=8.29 Hz, 1 H), 6.98 (s, 1 H), 6.93 (d, J=8.29 Hz, 1 H), 3.81 (s, 3 H), 3.79 (s, 3 H), 3.78 (s, 3 H).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09394285B2
出典データセットuspto-grants-2016_07
ORD IDord-658b7da7139e41e58fb7df083e94b628
出典メモuspto-grants-2016_07