戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1784299作成日:2026年10月26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/1784299

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Ethylacetate methanolHCID 21584119—
生成物Methyl 4-amino-3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)benzoateHCID 1196207783%

反応条件

温度20 °C

反応手順

Methyl 3-({3-[(tert-butoxycarbonyl)amino]propyl}amino)-4-nitrobenzoate (10.2 g) in solution in a mixture of ethyl acetate/methanol 3:1 (300 ml), and 10% palladium on carbon (1.02 g) are introduced into an autoclave. After stirring for 4 hours under a hydrogen atmosphere (3 bar) at a temperature of approximately 20° C., the catalyst is eliminated by filtration on celite and the filtrate is concentrated under reduced pressure at 40° C. in order to produce the expected compound in the form of an oil (7.75 g; 83% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07501525B2
出典データセットuspto-grants-2009_03
ORD IDord-738362d4b1254d849c6196150c37dc39
出典メモuspto-grants-2009_03