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HRID 1914921作成日:2026年10月24日

tert-Butyl (2-((5-methoxy-2-nitrophenyl)amino)ethyl)carbamate → Carbamic acid, N-[2-[(2-amino-5-methoxyphenyl)amino]ethyl]-, 1,1-dimethylethyl ester

https://huagongshe.com/ja/reaction/1914921

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl (2-((5-methoxy-2-nitrophenyl)amino)ethyl)carbamateHCID 59345555—
触媒Palladium hydroxideHCID 9942167—
溶媒1,4-DioxaneHCID 31275—
生成物Carbamic acid, N-[2-[(2-amino-5-methoxyphenyl)amino]ethyl]-, 1,1-dimethylethyl esterHCID 59345530—

反応手順

A 2 L round bottom flask equipped with a stir bar was charged with a suspension of 20% Pd(OH)2 (5 g) and 1,4-dioxane (800 mL). [2-(5-Methoxy-2-nitrophenylamino)-ethyl]-carbamic acid tert-butyl ester (100 g, 0.32 mol) was added to the suspension. The reaction mixture was hydrogenated (balloon) for 48 h (until the starting material had been consumed) followed by the addition of K2CO3 (100 g) was added to the mixture and stirred for an additional 12 h to remove traces of water. The suspension was filtered to remove the Pd(OH)2 and K2CO3. The filtrate was used in the next step without further purification (yield not determined).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08614243B2
出典データセットuspto-grants-2013_12
ORD IDord-0e288ddbedd74940acb2275fc30710e2
出典メモuspto-grants-2013_12