HRID385880
反应详情
EQUATION
反应方程式
REACTANTS
反应物
HCID6228
N,N-Dimethylformamide
C3H7NO
HCID75771
1-Hydroxybenzotriazole
C6H5N3O
HCID81531
Diisopropylethylamine
C8H19N
HCID2050129
3-Bromopyridine-2-carboxylic Acid
C6H4BrNO2
HCID9886157
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
HCID13247046
5,6,7,8-Tetrahydroimidazo[1,2-a]pyrazine
C6H9N3
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
A solution of HOBt (148 mg, 0.97 mmol), DIEA (130 μL, 0.74 mmol), HATU (367 mg, 0.97 mmol), bromopyridine-2-carboxylic acid (150 mg, 0.74 mmol) and 5,6,7,8-tetrahydroimidazo[1,2-a]pyrazine (91 mg, 0.74 mmol) in DMF (2.5 mL) was stirred overnight at 65° C. Upon completion, Si-carbonate (2.8 g, 2.23 mmol) and DCM (3 mL) were added and the mixture was shaken overnight at room temperature. The resulting mixture was then filtered, washed with DCM, concentrated in vacuo and purified by reverse phase HPLC (acetonitrile/water+formic acid modifier) to afford the title compound.
WORKUP
后处理
- filtrationThe resulting mixture was then filtered
- washwashed with DCM
- concentrationconcentrated in vacuo
- custompurified by reverse phase HPLC (acetonitrile/water+formic acid modifier)