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HRID 378895作成日:2026年10月26日
Potassium Carbonate → (4-Bromo-2-methyl-phenyl)-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanone
https://huagongshe.com/reaction/378895
関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 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-methylbenzoyl chloride | HCID 12846483 | — |
| 溶媒 | Dimethylformamide | HCID 6228 | — |
| 溶媒 | Diethylformamide | HCID 12051 | — |
| 生成物 | (4-Bromo-2-methyl-phenyl)-(5,11-dihydro-pyrido[2,3-b][1,5]benzodiazepin-6-yl)-methanone | HCID 15547049 | 53.4% |
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 was added solid potassium carbonate (6.3 g, 45.6 mmol). A solution of the crude 4-bromo-2-methylbenzoyl chloride (22.8 mmol) in N,N-diethylformamide was added dropwise, and the mixture stirred at room temperature for 15 minutes. Excess potassium carbonate was filtered off, the filtrate was washed with water and the aqueous layer was extracted with chloroform. The extracts were dried over anhydrous sodium sulfate, evaporated to dryness and the residue dissolved in dichloromethane and absorbed onto a silica Merck-60 flash column. Elution with 20% ethyl acetate in hexane provided the title compound (3.2 g) as a foam which crystallized upon sonication from ethanol hexane.
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-15891177812a46ce937adeb4342eb50b |
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| 出典メモ | uspto-grants-2001_10 |
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