HRID15589
反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
PROCEDURE
实验过程
{5-[Benzyl-(3-chloro-benzoyl)-amino]-2-propyl-benzoimidazol-1-yl}-acetic acid tert-butyl ester (0.12 mmol) was treated with TFA (2 mL) for 2 hours, concentrated, and purified by preparative LCMS to give the title compound. 1H NMR (d6-DMSO) δ7.89 (m, 1H), 7.71 (m, 1H), 7.52 (m, 1H), 7.45 (m, 1H), 7.21 (m, 6H), 6.91 (m, 1H), 5.11 (s, 2H), 4.91 (s, 2H), 2.65 (t, 2H), 1.71 (m, 2H), 0.92 (t, 3H). MS calculated for C26H24ClN3O3+H: 462, observed: 462.
WORKUP
后处理
- concentrationconcentrated
- custompurified by preparative LCMS