関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ammonia | HCID 222 | — |
| 反応物 | Hydrochloric Acid | HCID 313 | — |
| 反応物 | Diazepam | HCID 3016 | — |
| 反応物 | Boron trifluoride etherate | HCID 8000 | — |
| 反応物 | Sodium borohydride | HCID 4311764 | — |
| 溶媒 | Tetrahydrofuran | HCID 8028 | — |
| 生成物 | Medazepam | HCID 4041 | 103% |
反応手順
To a suspension of 2.28 g of sodium borohydride in 35ml of tetrahydrofuran was added dropwise with stirring a solution of 13.0 g of boron trifluoride etherate in 10ml of tetrahydrofuran below 10° C, and the mixture was stirred at room temperature for 45 minutes. To the mixture was added dropwise solution of 1.43 g of 1-methyl-5-phenyl-7-chloro-1,3-dihydro-2H-1,4-benzodiazepin-2-one in 10 ml of tetrahydrofuran at -15° to -12.5° C over a period of 5 minutes, and then the mixture was stirred at =15° C for 22 hours. The reaction mixture was poured into 100 ml of ice-water, and then 20 ml of concentrated hydrochloric acid was added. The mixture was refluxed for 30 minutes, then cooled, and neutralized with concentrated ammonia. The tetrahydrofuran layer was separated, and the aqueous layer was extracted with ether. The combined organic layer was washed with water and dried over anhydrous sodium sulfate, and the solvent was removed under reduced pressure to obtain 1.4 g of 1-methyl-5-phenyl-7-chloro-2,3-dihydro-1H-1,4-benzodiazepine.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US04044003 |
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| 出典データセット | uspto-grants-1977_08 |
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| ORD ID | ord-f477172c64e844b98d04e50fc6afdfa7 |
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| 出典メモ | uspto-grants-1977_08 |
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