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HRID 1520606作成日:2026年10月26日

4-Chloro-3-nitrobenzenesulfonamide → 4-(4-Methylpiperazin-1-ylamino)-3-nitrobenzenesulfonamide

https://huagongshe.com/reaction/1520606

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chloro-3-nitrobenzenesulfonamideHCID 7324—
反応物N,N,N',N'-TetramethylethylenediamineHCID 8037—
反応物4-Methylpiperazin-1-ylamine dihydrochloride hydrateHCID 198221—
溶媒1,4-DioxaneHCID 31275—
生成物4-(4-Methylpiperazin-1-ylamino)-3-nitrobenzenesulfonamideHCID 4737741—

反応手順

A mixture of 4-chloro-3-nitrobenzenesulfonamide (1 g), 4-methylpiperazin-1-amine dihydrochloride (1 g) and N1,N1,N2,N2-tetramethylethane-1,2-diamine (3 mL) in dioxane (10 mL) was refluxed for 12 hours, cooled to ambient temperature and filtered. The filtrate was added to a silica gel column (Analogix, SF65-200 g) and purified by eluting with 1-5% methanol/dichloromethane).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09073855B2
出典データセットuspto-grants-2015_07
ORD IDord-335cab165f8c42b99ec0cfd2944e3443
出典メモuspto-grants-2015_07