戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 274957作成日:2026年10月25日

Triethylamine → 4-Amino-N-[1-((4-amino-3-nitro-phenyl)-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-3,5-dichlorobenzenesulphonamide

https://huagongshe.com/reaction/274957

反応式

関与物質

役割名称HCID仕込み量
反応物TriethylamineHCID 8471—
反応物4-Amino-3-nitro-phenylalanyl-(4-methyl-piperidine)HCID 18659293—
反応物4-Amino-3,5-dichlorobenzene-1-sulfonyl chlorideHCID 18975981—
溶媒DichloromethaneHCID 6344—
生成物4-Amino-N-[1-((4-amino-3-nitro-phenyl)-methyl)-2-(4-methyl-piperidin-1-yl)-2-oxo-ethyl]-3,5-dichlorobenzenesulphonamideHCID 20089042—

反応手順

3.06 g (10 mMol) of 4-amino-3-nitro-phenylalanyl-(4-methyl-piperidine) are dissolved in 100 ml of methylene chloride and combined with 2.8 ml (20 mMol) of triethylamine. Then at ambient temperature 3.1 g (12 mMol) of 4-amino-3,5-dichloro-benzenesulphonic acid chloride in 20 ml of methylene chloride is slowly added dropwise. After 2 hours the precipitate is suction filtered, washed with methylene chloride and dried at 70° C. For further purification the precipitate is suspended in 100 ml of ethanol, decocted and after cooling suction filtered again.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05391556
出典データセットuspto-grants-1995_02
ORD IDord-cffdfd0cd4324365967dd6d75102a36f
出典メモuspto-grants-1995_02