戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 41303作成日:2026年10月24日

Hydrochloric Acid → (2S)-2-methyl-1-(2-pyridinylcarbonyl)piperazine dihydrochloride

https://huagongshe.com/reaction/41303

反応式

関与物質

役割名称HCID仕込み量
反応物Hydrochloric AcidHCID 313—
反応物DiisopropylethylamineHCID 81531—
反応物Pyridine-2-carbonyl chlorideHCID 135034—
反応物(S)-1-Boc-3-methylpiperazineHCID 7023035—
反応物1,1-dimethylethyl (3S)-3-methyl-4-(2-pyridinylcarbonyl)-1-piperazinecarboxylateHCID 67221682—
溶媒WaterHCID 962—
溶媒DichloromethaneHCID 6344—
溶媒1,4-DioxaneHCID 31275—
生成物(2S)-2-methyl-1-(2-pyridinylcarbonyl)piperazine dihydrochlorideHCID 67222743100.1%

反応手順

To a solution 1,1-dimethylethyl (3S)-3-methyl-1-piperazinecarboxylate (140 mg, 0.699 mmol) in dichloromethane (5 ml) was added DIPEA (0.183 ml, 1.049 mmol) at room temperature. 2-pyridinecarbonyl chloride (104 mg, 0.735 mmol) was then added and the resultant mixture stirred for 3 h30. The reaction mixture was then diluted with a further 2 ml DCM and 5 ml of water were added and the layers separated, the organics were then washed with 5 ml 2M HCl solution and 5 ml sat NaHCO3 solution then dried (hydrophobic frit) and concentrated to dryness. To a solution of the resulting 1,1-dimethylethyl (3S)-3-methyl-4-(2-pyridinylcarbonyl)-1-piperazinecarboxylate (78 mg, 0.255 mmol) in 1,4-Dioxane (1 ml) was added HCl (4M in 1,4-Dioxane) (0.319 ml, 1.277 mmol) at room temperature and the resultant mixture stirred overnight at room temperature. Reaction mixture concentrated to dryness and solid triturated with diethylether to give the title compound (71 mg) used without further purification.

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-3ec05c3eb13147cc824496add55593c4
出典メモuspto-grants-2013_09