関与物質
| 役割 | 名称 | HCID | 仕込み量 |
|---|
| 反応物 | Ethyl Acetate | HCID 8857 | — |
| 反応物 | Trimethylsilyl iodide | HCID 85247 | — |
| 反応物 | methyl (2-methyl-3-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-4-yl)carbamate | HCID 57722308 | — |
| 溶媒 | Dichloromethane | HCID 6344 | — |
| 生成物 | 4-Amino-2-methyl-1,2,4,5-tetrahydro-2-benzazepin-3-one | HCID 57722303 | 57% |
反応手順
0.6 ml of trimethylsilyl iodide is added to a solution of 203 mg (0.93 mmol) of product 2 in 10 ml of dichloromethane, and the mixture is then refluxed for 3 hours. After cooling to room temperature and adding 50 ml of ethyl acetate, the organic phase is extracted with 2×25 ml of 1N hydrochloric acid solution. The aqueous phases are combined, cooled and then basified by addition of 5N sodium hydroxide. The basic aqueous phases are then saturated with NaCl, and then extracted with 3×25 ml of ethyl acetate. The organic phases are combined, dried over magnesium sulfate and evaporated under reduced pressure to give an oily residue. This residue is chromatographed on silica gel, eluting with a 90/10 dichloromethane/methanol mixture. 100 mg (57%) of the expected product 3 are obtained in the form of an oil.
情報源と証拠
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 特許番号 | US07550453B2 |
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| 出典データセット | uspto-grants-2009_06 |
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| ORD ID | ord-36c906b80d454134ba87a400e65e03f4 |
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| 出典メモ | uspto-grants-2009_06 |
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