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HRID 1358931作成日:2026年10月25日

tert-Butyl 4-(2-methoxy-5-nitrophenyl)piperazine-1-carboxylate → Tert-butyl 4-(5-amino-2-methoxyphenyl)piperazine-1-carboxylate

https://huagongshe.com/reaction/1358931

反応式

関与物質

役割名称HCID仕込み量
反応物tert-Butyl 4-(2-methoxy-5-nitrophenyl)piperazine-1-carboxylateHCID 18180062—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒EthanolHCID 702—
溶媒WaterHCID 962—
生成物Tert-butyl 4-(5-amino-2-methoxyphenyl)piperazine-1-carboxylateHCID 1068617899%

反応手順

A slurry of 10% palladium on carbon (10 g) in a solution of 4-tert-butoxycarbonyl-1-(2-methoxy-5-nitrophenyl)piperazine (D2) (124.5 g) in ethanol (3.5L) and water (50 ml) was stirred with hydrogen at ambient temperature and atmospheric pressure for 18 h. The reaction mixture was filtered and the filtrate concentrated to afford the title compound (D3) as a gum (112 g, 99%). MH+ 308.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US06599904B2
出典データセットuspto-grants-2003_07
ORD IDord-6b3e017198c046ea952784515861017e
出典メモuspto-grants-2003_07