反应详情
EQUATION
反应方程式
REACTANTS
反应物
Acetonitrile
C2H3N
1,4-Dioxane
C4H8O2
Diisopropylethylamine
C8H19N
2 次
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
1,2,3-Triazole-4-carboxylic acid
C3H3N3O2
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
(2S,4R)-4-Amino-5-biphenyl-4-yl-2-hydroxymethyl-2-methyl-pentanoic acid (76 mg, 242 μmol) in MeCN (0.4 mL, 8 mmol) and 4 M HCl in 1,4-dioxane (242 μL, 969 μmol) was combined with propan-1-ol (0.5 mL) at 60° C. The resulting mixture was stirred until solid precipitation was observed (˜30 minutes). The solvent was evaporated under vacuum and the solids were azeotroped in toluene and dried under vacuum. 1,2,3-Triazole-4-carboxylic acid (0.0274 g, 0.242 mmol), DIPEA (169 μL, 969 μmol) and HATU (92 mg, 242 μmol) were combined in DMF (0.2 mL) and stirred for 5 minutes at room temperature. This was then combined with the dried solids, predissolved in DMF (0.2 mL) and DIPEA (0.5 eq.). The resulting mixture was stirred for 15 minutes and the reaction was quenched with AcOH. The product was purified by preparative HPLC and lyophilized to yield the title compound (24 mg; purity 95%). MS m/z [M+H]+ calc'd for C25H30N4O4, 451.23. found 451.4.
WORKUP
后处理
- custom(˜30 minutes)
- customThe solvent was evaporated under vacuum
- customthe solids were azeotroped in toluene
- customdried under vacuum
- stirringstirred for 5 minutes at room temperature
- stirringThe resulting mixture was stirred for 15 minutes
- customthe reaction was quenched with AcOH
- customThe product was purified by preparative HPLC