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HRID 2232405作成日:2026年10月25日

N-{4-[4-(4-Nitropyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide → N-{4-[4-(4-Aminopyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide

https://huagongshe.com/reaction/2232405

反応式

関与物質

役割名称HCID仕込み量
反応物N-{4-[4-(4-Nitropyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamideHCID 21283530—
反応物HCID 178418361HCID 178418361—
触媒PalladiumHCID 23938—
溶媒MethanolHCID 887—
生成物N-{4-[4-(4-Aminopyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamideHCID 2128353559.7%

反応手順

A solution of N-{4-[4-(4-nitropyrid-2-yl)piperazin-1-yl]phenyl}methanesulphonamide (100 mg) in methanol (40 ml) was hydrogenated at 3 bar and 22° C. in the presence of 5% palladium on carbon (20 mg) until no more hydrogen was taken up. The catalyst was filtered off and the filtrate was evaporated. The residue was crystallised from aqueous methanol to give the title compound (55 mg), m.p. 225°-227° C. Found: C,55.50; H,6.04; N,19.66. C16H21N5O2S requires: C,55.31; H,6.09; N,20.16%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04788196
出典データセットuspto-grants-1988_11
ORD IDord-6871f8c47b3b466dbc9ba3ff4642ab27
出典メモuspto-grants-1988_11