HRID31403
反应详情
EQUATION
反应方程式
REACTANTS
反应物
HCID10824
3-Methoxyaniline
C7H9NO
HCID81531
Diisopropylethylamine
C8H19N
HCID9886157
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
HCID16086086
4-Methyl-3-(4,4,5,5-tetramethyl-1,3,2-dioxaborolan-2-yl)benzoic acid
C14H19BO4
2 次
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
4-Methyl-3-(4,4,5,5-tetramethyl-[1,3,2]dioxaborolan-2-yl)-benzoic acid (Intermediate 21) (2 g) was dissolved in dimethylformamide (20 ml). To this was added 3-methoxyaniline (0.985 g), di-isopropylethylamine (4 ml) and HATU (3.05 g). The mixture was stirred for 18 hours at room temperature. The solvent was removed in vacuo and the residue partitioned between ethyl acetate (250 ml) and water (50 ml). The organic layer was dried over magnesium sulfate, filtered and removed in vacuo to give the crude material. The product was purified using silica Biotage cartridge (90 g) eluting with 1:4 ethylacetate/cyclohexane to give a white solid (2.06 g, 5.61 mmol).
WORKUP
后处理
- customThe solvent was removed in vacuo
- customthe residue partitioned between ethyl acetate (250 ml) and water (50 ml)
- dry with materialThe organic layer was dried over magnesium sulfate
- filtrationfiltered
- customremoved in vacuo
- customto give the crude material
- customThe product was purified
- washeluting with 1:4 ethylacetate/cyclohexane