反应详情
EQUATION
反应方程式
REACTANTS
反应物
Water
H2O
1-Hydroxybenzotriazole
C6H5N3O
Diisopropylethylamine
C8H19N
6-Methylnicotinic acid
C7H7NO2
Methanaminium, N-[(1H-benzotriazol-1-yloxy)(dimethylamino)methylene]-N-methyl-, hexafluorophosphate(1-) (1:1)
C11H16F6N5OP
(S)-4-N-Boc-2-methylpiperazine
C10H20N2O2
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
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)
WORKUP
后处理
- customSolvent was removed by evaporation and EtOAc
- additionwas added to the residue
- extractionthe solution was extracted with saturated aqueous sodium bicarbonate and sodium chloride solutions
- customThe organic layer was evaporated to dryness
- dissolutiondissolved in dioxane (100 ml)
- stirringstirred with 4M HCl in dioxane (15 ml) and water (0.25 ml) overnight
- customThe solution was evaporated to dryness
- custompurified