戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 899907作成日:2026年10月25日

Tert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamate → Tert-butyl 3-[(2-amino-5-{[bis(3-methylbutyl)amino]carbonyl}phenyl)amino]propylcarbamate

https://huagongshe.com/reaction/899907

反応式

関与物質

役割名称HCID仕込み量
反応物Tert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamateHCID 68789966—
触媒PalladiumHCID 23938—
溶媒Ethanol ethylacetateHCID 21584252—
生成物Tert-butyl 3-[(2-amino-5-{[bis(3-methylbutyl)amino]carbonyl}phenyl)amino]propylcarbamateHCID 6879210089%

反応条件

温度20 °C

反応手順

Tert-butyl 3-[(5-{[bis(3-methylbutyl)amino]carbonyl}-2-nitrophenyl)amino]propylcarbamate (1.65 g) in solution in a mixture of ethyl acetate/ethanol 2:1 (130 ml), and 10% palladium on carbon (165 mg) are introduced into an autoclave. After stirring for 3 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 (1.35 g; 89% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07355052B2
出典データセットuspto-grants-2008_04
ORD IDord-fc03050bbe4e4c61a2716c9c81665cc9
出典メモuspto-grants-2008_04