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HRID 8098作成日:2026年10月24日

Potassium Carbonate → racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/ja/reaction/8098

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium CarbonateHCID 11430—
反応物BromoacetonitrileHCID 11534—
反応物{1-Methyl-2-[7-(benzyloxy)-1h-indol-3-yl]ethyl}-carbamic acid tert-butyl esterHCID 11485811—
溶媒Methyl Ethyl KetoneHCID 6569—
生成物racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl esterHCID 6951856570.2%

反応条件

温度80 °C

反応手順

The crude {1-methyl-2-[7-hydroxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester from above (29.2 g, 102 mmol theory) is dissolved in methyl ethyl ketone (300 mL) and bromoacetonitrile (20.4 mL, 306 mmol) and potassium carbonate (33.8 g, 250 mmol) is added. The mixture is heated at 80° C. for 2 hours. The solids are removed by filtration, the cake is washed with methyl ethyl ketone, and the combined filtrates are concentrated by rotary evaporation. The crude product is purified by flash chromatography (500 g silica gel, eluted with 8×500 mL dichloromethane, 4×500 mL 5% ethyl acetate/dichloromethane, 6×500 mL 10% ethyl acetate/dichloromethane). The fractions containing product are concentrated and hexane is added to the solution to precipitate out the product affording 23.7 g (70.2% yield) of racemic {1-methyl-2-[7-cyanomethoxy-1H-indol-3-yl]ethyl}-carbamic acid tert-butyl ester.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07087635B2
出典データセットuspto-grants-2006_08
ORD IDord-579ccc08061142699e0875fb06cf892e
出典メモuspto-grants-2006_08