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HRID 338444作成日:2026年10月27日

Dimethylformamide → 6-chloro-5-(5-phenylpyrazin-2-yl)-1H-indole-3-carbaldehyde

https://huagongshe.com/reaction/338444

反応式

関与物質

役割名称HCID仕込み量
反応物DimethylformamideHCID 6228—
反応物Potassium CarbonateHCID 11430—
反応物Chloro-N,N-dimethylformiminium chlorideHCID 77311—
反応物2-Chloro-5-phenylpyrazineHCID 1236664—
反応物6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indoleHCID 86698733—
生成物6-chloro-5-(5-phenylpyrazin-2-yl)-1H-indole-3-carbaldehydeHCID 86698775—

反応条件

温度30 °C

反応手順

To a 0.4M solution of chlormethylene dimethylammonium chloride in DMF (7.5 mL, 3.8 mmol) was added 6-chloro-5-(5,5-dimethyl-1,3,2-dioxaborinan-2-yl)-1H-indole (493 mg, 1.88 mmol). The mixture was stirred at 30° C. for 2 hrs. 0.50 mL of this solution (0.15 mmol) was placed in a vial with a 0.3M solution of 2-chloro-5-phenylpyrazine in DMF (0.50 mL, 0.15 mmol). 2M potassium carbonate (0.30 mL, 0.60 mmol) was then added and the mixture purged with nitrogen. PddppfCl2 (9 mg, 0.01 mmol) was then added and the vial capped and heated to 90° C. for 3 hours. The reaction mixture was concentrated by Speedvac and purified via preparative TLC to give the title compound that was taken forward without further purification.

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-90552355b19948d2b1ad3b1965bd6359
出典メモuspto-grants-2014_11