돌아가기
Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 43373생성일: 2026년 10월 24일

Water → (2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazine

https://huagongshe.com/ko/reaction/43373

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물1-HydroxybenzotriazoleHCID 75771—
반응물DiisopropylethylamineHCID 81531—
반응물6-Methylnicotinic acidHCID 137860—
반응물Methanaminium, N-((1H-benzotriazol-1-yloxy)(dimethylamino)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)HCID 2733084—
반응물(S)-1-Boc-3-methylpiperazineHCID 7023035—
용매DimethylformamideHCID 6228—
생성물(2S)-2-Methyl-1-[(6-methyl-3-pyridinyl)carbonyl]piperazineHCID 591613781,394.9%

반응 단계

To a solution of 1,1-dimethylethyl (3S)-3-methyl-1-piperazinecarboxylate (1 g, 4.99 mmol) in DMF (5 ml) was added 6-methyl-3-pyridinecarboxylic acid (0.685 g, 0.340 mmol), HOBT.H2O (0.765 g, 4.99 mmol) and HBTU (1.894 g, 4.99 mmol). Finally DIPEA (2.62 ml, 14.98 mmol) was added and the reaction mixture was stirred at room temperature for 20 hours. Solvent was removed by evaporation and EtOAc was added to the residue and the solution was extracted with saturated aqueous sodium bicarbonate and sodium chloride solutions. The organic layer was evaporated to dryness and dissolved in dioxane (100 ml) and stirred with 4M HCl in dioxane (15 ml) and water (0.25 ml) overnight. The solution was evaporated to dryness and purified using an ion exchange column (SCX, Biotage) to give the title compound as an oil (1.04 g)

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08536183B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-72d4c1c2e2d642058b9a80973bd0f26e
출처 메모uspto-grants-2013_09