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HRID 629599作成日:2026年10月26日

4-Chloro-3-nitrobenzenesulfonamide → 4-[1-(2-Methoxy-ethyl)-piperidin-4-ylamino]-3-nitro-benzenesulfonamide

https://huagongshe.com/reaction/629599

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TriethylamineHCID 8471—
反応物1-(2-Methoxyethyl)piperidin-4-amineHCID 20119121—
溶媒1,4-DioxaneHCID 31275—
生成物4-[1-(2-Methoxy-ethyl)-piperidin-4-ylamino]-3-nitro-benzenesulfonamideHCID 68406613—

反応条件

温度90 °C

反応手順

1-(2-Methoxy-ethyl)-piperidin-4-ylamine (2.01 g) and triethylamine (3.24 mL, 2.35 g) were added to 1,4-dioxane (60 mL). 4-Chloro-3-nitrobenzenesulfonamide (2.50 g) was added, and the mixture was heated to 90° C. for 16 hours. The mixture was cooled and the material purified by flash column chromatography on silica gel using 10% methanol in dichloromethane.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US09315488B2
出典データセットuspto-grants-2016_04
ORD IDord-1158022bd4ec41c8aca24c74d2ca769e
出典メモuspto-grants-2016_04