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HRID 500102作成日:2026年10月26日

{2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-nitro-phenyl)-ethylcarbamoyl]-ethyl} carbamic acid tert-butyl ester → {2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-amino-phenyl)-ethylcarbamoyl]-ethyl}-carbamic acid tert-butyl ester

https://huagongshe.com/reaction/500102

反応式

関与物質

役割名称HCID仕込み量
反応物{2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-nitro-phenyl)-ethylcarbamoyl]-ethyl} carbamic acid tert-butyl esterHCID 68657947—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物{2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-amino-phenyl)-ethylcarbamoyl]-ethyl}-carbamic acid tert-butyl esterHCID 68657871—

反応手順

{2-(4-Hydroxy-phenyl)-1-[1-methylcarbamoyl-2-(4-nitro-phenyl)-ethylcarbamoyl]-ethyl}carbamic acid tert-butyl ester (300, 0.617 mmol) is dissolved in methanol (10 mL). To this was added palladium on carbon (10% by weight, 100 mg). The reaction is placed under a hydrogen atmosphere until reaction is complete (tlc). The catalyst is removed by filtration and the filtrate is concentrated to provide the amine, which is used without purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07769575B2
出典データセットuspto-grants-2010_08
ORD IDord-0d09edfc7d5a45708ad6f556debc364c
出典メモuspto-grants-2010_08