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HRID 609732作成日:2026年10月26日

5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole → 5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole

https://huagongshe.com/reaction/609732

反応式

関与物質

役割名称HCID仕込み量
反応物5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindoleHCID 19600443—
反応物4-Tributylstannyl-3,4-dihydropyranHCID 19600452—
溶媒TolueneHCID 1140—
生成物5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindoleHCID 1960044817%

反応手順

A solution of 5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole (Example 5a, 180 mg 0.48 mmol), 4-tributylstannyl-3,4-dihydropyran (180 mg, 0.48 mmol) and tetrakistriphenyphosphine palladium (118 mg, 0.1 mmol) in toluene (3 mL) was stirred at 100-110° C. A second portion of catalyst was added after 1 h and heating was continued overnight. After removal of the solvent in vacuo, flash chromatography on silica gel (2-6% 2M methanolic ammonia in dichloromethane) yielded 5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole (30.5 mg, 17%).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05998438
出典データセットuspto-grants-1999_12
ORD IDord-1f04ef2904a540abb5f21fe0815090e6
出典メモuspto-grants-1999_12