反应详情
EQUATION
反应方程式
REACTANTS
反应物
Benzyl alcohol
C7H8O
Hydrochloric Acid
ClH
N,N-Dimethylformamide
C3H7NO
1,4-Dioxane
C4H8O2
Diisopropylethylamine
C8H19N
Methanaminium, N-((dimethylamino)(3H-1,2,3-triazolo(4,5-b)pyridin-3-yloxy)methylene)-N-methyl-, hexafluorophosphate(1-) (1:1)
C10H15F6N6OP
未命名化合物
未命名化合物
PRODUCTS
生成物
PROCEDURE
实验过程
A mixture of (2R,4R)-4-amino-5-(3′-chlorobiphenyl-4-yl)-2-hydroxypentanoic acid ethyl ester (150.0 mg, 431 μmol), benzyl alcohol (446.2 μL, 4.3 mmol), and 4.0 M HCl in 1,4-dioxane (431 μL, 1.7 mmol) was stirred at room temperature overnight, then at 50° C. for 1 hour. The mixture was then concentrated under reduced pressure. 5-Hydroxy-1-pyridin-2-yl-1H-pyrazole-3-carboxylic acid (44.2 mg, 216 μmol) and HATU (98.4 mg, 259 mol) were stirred in DMF (0.5 mL, 5 mmol) for 10 minutes, then added to the concentrated mixture, along with DIPEA (113 μL, 647 μmol). The resulting mixture was stirred at room temperature for 2 hours and concentrated under reduced pressure. The residue was dissolved in 50% AcOH-water (5 mL), filtered, and purified by reverse phase preparative HPLC to yield the title compound (19.5 mg).
WORKUP
后处理
- waitat 50° C. for 1 hour
- concentrationThe mixture was then concentrated under reduced pressure
- stirringThe resulting mixture was stirred at room temperature for 2 hours
- concentrationconcentrated under reduced pressure
- dissolutionThe residue was dissolved in 50% AcOH-water (5 mL)
- filtrationfiltered
- custompurified by reverse phase preparative HPLC