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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 41303생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/41303

반응식

참여 물질

역할이름HCID투입량
반응물Hydrochloric AcidHCID 313—
반응물DiisopropylethylamineHCID 81531—
반응물Pyridine-2-carbonyl chlorideHCID 135034—
반응물(S)-1-Boc-3-methylpiperazineHCID 7023035—
반응물1,1-dimethylethyl (3S)-3-methyl-4-(2-pyridinylcarbonyl)-1-piperazinecarboxylateHCID 67221682—
용매WaterHCID 962—
용매DichloromethaneHCID 6344—
용매1,4-DioxaneHCID 31275—
생성물(2S)-2-methyl-1-(2-pyridinylcarbonyl)piperazine dihydrochlorideHCID 67222743100.1%

반응 단계

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.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08530478B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-3ec05c3eb13147cc824496add55593c4
출처 메모uspto-grants-2013_09