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HRID 41302作成日:2026年10月24日

4-Chlorobenzenesulfonyl chloride → (3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazine

https://huagongshe.com/ja/reaction/41302

反応式

関与物質

役割名称HCID仕込み量
反応物4-Chlorobenzenesulfonyl chlorideHCID 7398—
反応物TriethylamineHCID 8471—
反応物tert-Butyl (2R)-2-methylpiperazine-1-carboxylateHCID 10262201—
溶媒DichloromethaneHCID 6344—
生成物(3R)-1-[(4-chlorophenyl)sulfonyl]-3-methylpiperazineHCID 1163046578.7%

反応手順

To a solution of 1,1-dimethylethyl (2R)-2-methyl-1-piperazinecarboxylate (1.5 g, 07.5 mmol) in dry DCM (40 mL) was added triethylamine (2.59 mL, 18.8 mmol) and 4-chlorobenzenesulfonyl chloride (3.15 g, 10.5 mmol) and the reaction stirred at room temperature for 48 h. To the reaction was added resin supported-triamine (5 g) and the mixture stirred for 4 h. The reaction mixture was filtered and the filtrate washed with 0.5 M HCl (aq., 100 mL) followed by water (100 mL) before it was dried (MgSO4), filtered and the solvent removed in vacuo. The crude product was dissolved in DCM (40 mL) and TFA (10 mL) was added. The solution was stirred for 20 min. The solvent was evaporated and the residue tajen up in DCM (40 mL) and washed with 50% aqueous sodium bicarbonate (100 mL) followed by water (100 mL). The organic phase was dried (MgSO4), filtered and the solvent removed in vacuo to give the title compound (1.62 g).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08530478B2
出典データセットuspto-grants-2013_09
ORD IDord-d72421402bcd411a95caa05e81703400
出典メモuspto-grants-2013_09