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HRID 633514作成日:2026年10月27日

Cesium fluoride → 7-methoxy-3-(2-phenoxyphenyl)-1H-pyrrolo[2,3-c]pyridine

https://huagongshe.com/reaction/633514

反応式

関与物質

役割名称HCID仕込み量
反応物Cesium fluorideHCID 25953—
反応物(2-Phenoxyphenyl)boronic acidHCID 2773559—
反応物3-Iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridineHCID 53412719—
触媒HCID 178418397HCID 178418397—
溶媒MethanolHCID 887—
生成物7-methoxy-3-(2-phenoxyphenyl)-1H-pyrrolo[2,3-c]pyridineHCID 9041667338.6%

反応条件

温度120 °C

反応手順

A mixture of 3-iodo-7-methoxy-1H-pyrrolo[2,3-c]pyridine (0.274 g, 1.0 mmol), 2-phenoxyphenylboronic acid (0.278 g, 1.3 mmol, 1.3 equivalents), Pd(PPh3)4 (0.058 g, 0.05 mmol), and cesium fluoride (0.456 g, 3 mmol) in dimethxoyethane (3 mL) and methanol (1.5 mL) was heated under microwave conditions (120° C., 30 minutes). The reaction mixture was partitioned between water and ethyl acetate. The aqueous layer was extracted three times with ethyl acetate. The combined organic layers were washed with saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, filtered, and concentrated. The residue was purified by flash column chromatography (silica gel, 30% ethyl acetate/hexanes) to give the title compound (0.122 g, 38.6% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09321764B2
出典データセットuspto-grants-2016_04
ORD IDord-c490091761d54383a603ffe9a2da55ae
出典メモuspto-grants-2016_04