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5-bromo-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole → 5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole
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-benzoylindole | HCID 19600443 | — |
| 反応物 | 4-Tributylstannyl-3,4-dihydropyran | HCID 19600452 | — |
| 溶媒 | Toluene | HCID 1140 | — |
| 生成物 | 5-(3,4-dihydropyran-4-yl)-3-[2-(N,N-dimethylamino)ethyl]-1-benzoylindole | HCID 19600448 | 17% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 特許番号 | US05998438 |
| 出典データセット | uspto-grants-1999_12 |
| ORD ID | ord-1f04ef2904a540abb5f21fe0815090e6 |
| 出典メモ | uspto-grants-1999_12 |