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HRID 890506作成日:2026年10月27日

Water → 2-[(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)amino]-N-cyclohexyl-N-phenylacetamide

https://huagongshe.com/reaction/890506

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物N-CyclohexylanilineHCID 74567—
反応物Lithium HexamethyldisilazideHCID 2733832—
反応物2-chloro-N-(1,3,3-trimethylbicyclo[2,2,1]hept-2-yl)acetamideHCID 22251091—
溶媒TetrahydrofuranHCID 8028—
生成物2-[(1,3,3-trimethylbicyclo[2.2.1]hept-2-yl)amino]-N-cyclohexyl-N-phenylacetamideHCID 2802703—

反応条件

温度0 °C

反応手順

To a solution of N-cyclohexylaniline (100 mg, 0.56 mmol) in tetrahydrofuran (4 ml) at −78° C. was added LiHMDS (1 ml of a 1M solution in tetrahydrofuran) dropwise. The solution was allowed to warm to 0° C., then recooled to −78° C., and a solution of 2-chloro-N-(1,3,3-trimethylbicyclo[2,2,1]hept-2-yl)acetamide (124 mg, 0.56 mmol) in tetrahydrofuran (1 ml) added dropwise. The mixture was allowed to warm to room temperature, and was stirred for 1 hour. Water was added, and the mixture was extracted with ethyl acetate. The organic layer was washed with brine, and dried over magnesium sulfate. The ethyl acetate solution was absorbed onto silica gel, which was eluted with 3% methanol/methylene chloride, to yield N-cyclohexyl-N-phenyl-2-(1,3,3-trimethyl-bicyclo[2.2.1]hept-2-ylamino)-acetamide.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06995285B2
出典データセットuspto-grants-2006_02
ORD IDord-ac59e46a7a7e4ba19be4a36a44a1572f
出典メモuspto-grants-2006_02