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HRID 64453作成日:2026年10月27日

Water → methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate

https://huagongshe.com/reaction/64453

反応式

関与物質

役割名称HCID仕込み量
反応物WaterHCID 962—
反応物DimethylformamideHCID 6228—
反応物Silane, ((1-methoxy-2-methyl-1-propenyl)oxy)trimethyl-HCID 552336—
反応物(S)-N-Boc-1-(3-bromophenyl)ethylamineHCID 56971804—
触媒Zinc(II) fluorideHCID 10129912—
触媒HCID 178418851HCID 178418851—
溶媒Ethyl AcetateHCID 8857—
生成物methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoateHCID 86713467—

反応条件

温度100 °C

反応手順

A mixture of 1 g of tert-butyl[(1S)-1-(3-bromophenyl)ethyl]carbamate, 18 mg of bis(tri-tert-butylphosphine)palladium (0), 180 mg of zinc fluoride, 1 ml of [(1-methoxy-2-methylpropa-1-en-1-yl)oxy](trimethyl)silane, and 10 ml of DMF was stirred at 80° C. overnight and at 100° C. for 5 hours. 25 mg of bis(tri-tert-butylphosphine)palladium (0) and 0.34 ml of [(1-methoxy-2-methylpropa-1-en-1-yl)oxy](trimethyl)silane were added thereto, followed by stirring at 80° C. for 3 days. To the reaction mixture were added water and ethyl acetate to carry out a layer separation operation. The organic layer was washed with water and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The obtained residue was purified by silica gel column chromatography to obtain 281 mg of methyl 2-(3-{(1S)-1-[(tert-butoxycarbonyl)amino]ethyl}phenyl)-2-methylpropanoate.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09447090B2
出典データセットuspto-grants-2016_09
ORD IDord-647d358395324543b17b84fbbf089926
出典メモuspto-grants-2016_09