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HRID 1521685作成日:2026年10月25日

Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate → Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoate

https://huagongshe.com/reaction/1521685

反応式

関与物質

役割名称HCID仕込み量
反応物Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoateHCID 67235341—
触媒PalladiumHCID 23938—
溶媒Ethyl AcetateHCID 8857—
生成物Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 1196207780%

反応手順

A stirred suspension of methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate (6.5 g, 18.4 mmol) in ethyl acetate (500 mL) is hydrogenated over 10% palladium on carbon (2.6 g) under balloon pressure for 4 h. The catalyst is removed by filtration through Celite, washing well with ethyl acetate. The solvent is evaporated to afford the title compound (4.72 g, 80%) as a white solid. LCMS (Method T) 1.39 min, 324.70 (MH+).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073926B2
出典データセットuspto-grants-2015_07
ORD IDord-643ca5a2ebb147999dd8196d19ffdd6f
出典メモuspto-grants-2015_07