関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | trimethylsilyl N-trimethylsilylethanimidate | HCID 25248 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 1-cyclopentyl-1,5-dihydro-4H-pyrrolo[3,2-c]pyridin-4-one | HCID 117987824 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 3-bromo-1-cyclopentyl-1,5-dihydro-4H-pyrrolo[3,2-c]pyridin-4-one | HCID 117988493 | 69.4% |
反応手順
To a solution of 1-cyclopentyl-1,5-dihydro-4H-pyrrolo[3,2-c]pyridin-4-one (3.40 g) in DMF (42.0 mL) was added trimethylsilyl N-(trimethylsilyl)ethanimidate (7.52 g) at room temperature, and the mixture was stirred at 40° C. for 3 hr. The reaction mixture was allowed to be cooled to room temperature, and NBS (3.59 g) was added thereto at room temperature. The reaction mixture was stirred overnight at room temperature, water was added thereto, and the mixture was stirred at room temperature for 2 hr. The white precipitate was collected by filtration, and dried under reduced pressure to give the title compound (3.28 g).
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US09371320B2 |
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| 出典データセット | uspto-grants-2016_06 |
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| ORD ID | ord-f96fa7a44c5d4f9cb7b5f2f9ff9ae4cd |
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| 出典メモ | uspto-grants-2016_06 |
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