関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | N-bromobutanimide | HCID 67184 | — |
| 反応物 | 1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one | HCID 13694564 | — |
| 反応物 | Acetone diethylether | HCID 21584533 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | 9-Bromo-1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one | HCID 52937041 | — |
反応手順
To a solution of 1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one (9.1 g, 48.6 mmol) in 100 ml dry DMF was added dropwise a solution of N-bromosuccinimide (9.08 g, 51.0 mmol) in 150 ml dry DMF at 0° C. The mixture was stirred at 0° C. for 2 h, then 400 ml water was added and the solution was extracted with ethyl acetate (3×150 ml). The organic phase was washed with water (2×200 ml), then dried over MgSO4 and evaporated, affording a yellow solid, which was purified by crystallization from acetone/ether providing pure 9-bromo-1,2,6,7-tetrahydro-5H-pyrido[3,2,1-ij]quinolin-3-one (6.53, 24.5 mmol, 50%) as pale yellow needles.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US08541404B2 |
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| 出典データセット | uspto-grants-2013_09 |
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| ORD ID | ord-8b70a52ca51748fc840115cb32727ed2 |
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| 出典メモ | uspto-grants-2013_09 |
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