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HRID 1054681作成日:2026年10月25日

Ethyl Acetate → methyl 6-chloro-5-{4-[2-(piperazin-1-yl)ethoxy]phenyl}-1H-indole-3-carboxylate

https://huagongshe.com/reaction/1054681

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Potassium CarbonateHCID 11430—
反応物1-(2-(4-Bromophenoxy)ethyl)piperazineHCID 23325337—
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Toluene ethanolHCID 21863594—
生成物methyl 6-chloro-5-{4-[2-(piperazin-1-yl)ethoxy]phenyl}-1H-indole-3-carboxylateHCID 8669868464.4%

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 (80 mg, 0.15 mmol), 1-(2-(4-bromophenoxy)ethyl)piperazine (86 mg, 0.30 mmol), 2.0 M aqueous potassium carbonate (0.50 mL, 1.0 mmol), and Pd(dppf)Cl2 (10 mg, 0.01 mmol) in toluene/ethanol (1.44 mL/0.48 mL) was stirred at 110° C. for 2.5 hours. The mixture was poured into ethyl acetate and washed with water. The organic phase was dried over sodium sulfate, filtered, and concentrated in vacuo to give a residue, which was purified by preparative TLC to give the title compound (40 mg, 40% yield) as a white solid. 1H NMR (400 MHz, CDCl3): δ8.50 (s, 1 H), 8.10 (s, 1 H), 7.98 (s, 1 H), 7.55 (m, 1 H), 7.45 (m, 2 H), 7.00 (m, 2 H), 4.20 (m, 2 H), 3.90 (s, 3 H), 2.99 (m, 4 H), 2.85 (m, 2 H), 2.60 (m, 4 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-3f60ca154ce5409697c81f8cb072bd13
出典メモuspto-grants-2016_07