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HRID 338423作成日:2026年10月26日

Potassium Carbonate → tert-butyl 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenyl]pyrrolidine-1-carboxylate

https://huagongshe.com/reaction/338423

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物tert-Butyl 2-(4-bromophenyl)pyrrolidine-1-carboxylateHCID 53407516—
反応物6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indoleHCID 86698733—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒1,4-dioxane N,N-dimethylformamideHCID 21712069—
生成物tert-butyl 2-[4-(6-chloro-3-formyl-1H-indol-5-yl)phenyl]pyrrolidine-1-carboxylateHCID 8669875872.2%

反応手順

To a suspension of 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (150 mg, 0.57 mmol) in mixture solvent of 1,4-dioxane/N,N-dimethylformamide (5:1, 3 mL) was added vilsmeier salt (165 mg, 1.71 mmol) under nitrogen. The mixture was stirred at room temperature for 30 minutes under nitrogen. Potassium carbonate (2.0M in water, 1.5 mL) was added and stirred for 10 minutes, followed by the addition of tert-butyl 2-(4-bromophenyl)pyrrolidine-1-carboxylate (180 mg, 0.55 mmol), the mixture was degassed with nitrogen for 10 min., then treated with Pd(dppf)Cl2 (62 mg, 0.086 mmol). The reaction mixture was stirred at 90° C. for 30 minutes. The mixture was filtered through a Celite pad and the filtrate was partitioned between ethyl acetate (10 mL) and water (20 mL). The aqueous phase was extracted two times with ethyl acetate (10 mL), the combined organic layers were washed with brine (15 mL), dried over sodium sulfate, filtrated, and concentrated to afford crude product which was purified by silica-gel chromatography to give the title compound (170 mg, 72.2% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08889730B2
出典データセットuspto-grants-2014_11
ORD IDord-4e1ba4157b2045db8d94b7bb89c79cee
出典メモuspto-grants-2014_11