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HRID 1820889作成日:2026年10月27日

Sodium hydride → [3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-naphthalen-1-yl)-methanone

https://huagongshe.com/reaction/1820889

反応式

関与物質

役割名称HCID仕込み量
反応物Sodium hydrideHCID 24758—
反応物1-Naphthalenecarbonyl chloride, 2-ethoxy-HCID 108679—
反応物3-(3,4-dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridineHCID 11673285—
溶媒DimethylformamideHCID 6228—
生成物[3-(3,4-Dimethoxy-phenyl)-pyrrolo[2,3-b]pyridin-1-yl]-(2-ethoxy-naphthalen-1-yl)-methanoneHCID 1158328570.4%

反応手順

3-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine 1 (638 mg, 2.51 mmole) was dissolved in DMF (30 mL) and sodium hydride (60% dispersion in mineral oil, 100 mg, 2.50 mmole) was added in small portions to the reaction mixture. After stirring for 30 minutes, 2-ethoxy-1-naphthoyl chloride (646 mg, 2.76 mmole) was added and the reaction was stirred for 4 hours. The reaction mixture was poured into 200 mL of ice water and was extracted with ethyl acetate. The organic layer was washed with saturated bicarbonate solution followed by saturated potassium hydrogen sulfate and then brine. The resulting solution was dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The residue was purified by silica gel chromatography (30% ethyl acetate:hexanes) to yield 800 mg (70%) of the titled compound as a white solid MS(ESI) [M+H+]+=453.06.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07605168B2
出典データセットuspto-grants-2009_10
ORD IDord-57c9ad57aeee40adb993f07128b8d86d
出典メモuspto-grants-2009_10