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HRID 1986533作成日:2026年10月27日

Ethyl Acetate → 4-Amino-2-methyl-1,2,4,5-tetrahydro-2-benzazepin-3-one

https://huagongshe.com/reaction/1986533

反応式

関与物質

役割名称HCID仕込み量
反応物Ethyl AcetateHCID 8857—
反応物Trimethylsilyl iodideHCID 85247—
反応物methyl (2-methyl-3-oxo-2,3,4,5-tetrahydro-1H-2-benzazepin-4-yl)carbamateHCID 57722308—
溶媒DichloromethaneHCID 6344—
生成物4-Amino-2-methyl-1,2,4,5-tetrahydro-2-benzazepin-3-oneHCID 5772230357%

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

DOI10.6084/m9.figshare.5104873.v1
特許番号US07550453B2
出典データセットuspto-grants-2009_06
ORD IDord-36c906b80d454134ba87a400e65e03f4
出典メモuspto-grants-2009_06