関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Water | HCID 962 | — |
| 反応物 | Potassium Carbonate | HCID 11430 | — |
| 反応物 | 6,11-dihydro-5H-pyrido[2,3-b][1,5]benzodiazepine | HCID 11030760 | — |
| 反応物 | 4-Bromo-2-chlorobenzoyl chloride | HCID 15592207 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 生成物 | (4-Bromo-2-chloro-phenyl)-(5,11-dihydro-pyrido [2,3-b][1,5] benzodiazepin-10-yl)-methanone | HCID 21696873 | 53.9% |
反応手順
To a solution of 6,11-dihydro-5H-pyrido[2,3-b][1,5] benzodiazepine (3 g, 15.2 mmol) in N,N-dimethylformamide under nitrogen were added solid potassium carbonate (6.3 g, 45.6 mmol). The mixture was treated dropwise with a solution of the crude 4-bromo-2-chlorobenzoyl chloride (22.9 mmol) in N,N-dimethylformamide. After stirring at room temperature for 15 minutes, water was added under stirring. The resulting solid was collected, dissolved in chloroform, and the solution washed with 1N NaOH and brine. The organic layer was dried over anhydrous sodium sulfate and evaporated to dryness. The residue (purple foam) was dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided 3.4 g of the title compound as a foam which crystallized as a white solid by trituration from ethanol-ether, m.p. 165-168° C.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US06297234B1 |
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| 出典データセット | uspto-grants-2001_10 |
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| ORD ID | ord-cbe60203604a4ead849d41dddccd377c |
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| 出典メモ | uspto-grants-2001_10 |
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