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HRID 18194作成日:2026年10月26日

1,2-Dimethoxyethane → 1-[5-fluoro-3-(3-fluoro-benzyl)-7-(1-triisopropylsilanyl-1H-pyrrol-3-yl)-benzofuran-2-yl]-ethanone

https://huagongshe.com/reaction/18194

反応式

関与物質

役割名称HCID仕込み量
反応物1,2-DimethoxyethaneHCID 8071—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物1-(Triisopropylsilyl)pyrrole-3-boronic acidHCID 2763303—
反応物7-Bromo-5-fluoro-3-(3-fluoro-benzyl)-benzofuranHCID 59344909—
触媒Bis(cyclopenta-1,4-dien-1-yl(diphenyl)phosphane);dichloropalladium;iron(2+)HCID 178418228—
溶媒WaterHCID 962—
生成物1-[5-fluoro-3-(3-fluoro-benzyl)-7-(1-triisopropylsilanyl-1H-pyrrol-3-yl)-benzofuran-2-yl]-ethanoneHCID 5934491075%

反応条件

温度70 °C

反応手順

To a flask was added 7-bromo-5-fluoro-3-(3-fluoro-benzyl)-benzofuran (0.365 gm, 1.0 mmol), [1,1′-bis(diphenylphosphino)ferrocene]dichloropalladium (0.010 gm, 0.012 mmol), potassium phosphate (0.425 gm, 2.0 mmol), 1-(triisopropylsilyl)pyrrole-3-boronic acid (0.365 gm, 1.37 mmol), DME (12 ml) and water (2 ml). The mixture was evacuated and refilled with nitrogen while being sonicated. The mixture was heated in a microwave reactor for 15 minutes at 70° C., then for 15 minutes at 100° C., and then for 15 minutes at 130° C. The mixture was cooled, concentrated under reduced pressure, diluted with brine and extracted with ethyl acetate. The organic phase was absorbed onto a pad of silica gel that was rinsed with ethyl acetate/hexanes (250 ml, 1/9) and eluted to give 1-[5-fluoro-3-(3-fluoro-benzyl)-7-(1-triisopropylsilanyl-1H-pyrrol-3-yl)-benzofuran-2-yl]-ethanone (0.38 gm, 75% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07741326B2
出典データセットuspto-grants-2010_06
ORD IDord-769ada0d2a334d929efe39d644428bb9
出典メモuspto-grants-2010_06