反应详情
EQUATION
反应方程式
REACTANTS
反应物
PRODUCTS
生成物
AUXILIARIES
试剂、催化剂与溶剂
PROCEDURE
实验过程
To a solution of methyl 1-[2-(3-{5-[3-cyano-4-(2-methylpropyl)phenyl]-1,3,4-thiadiazol-2-yl}-2-ethylphenyl)ethyl]-3-azetidinecarboxylate (D32) (59 mg) in isopropanol (3 mL) and water (3 mL) was added sodium hydroxide (50 mg). The reaction mixture was stirred at room temperature for 1 h. The reaction mixture was neutralized with 1 M HCl solution. The solvent was removed in vacuo. The residue was dissolved in THF, and filtered. The filtrate was purified by Mass Directed AutoPrep to give 1-[2-(3-{5-[3-cyano-4-(2-methylpropyl)phenyl]-1,3,4-thiadiazol-2-yl}-2-ethylphenyl)ethyl]-3-azetidinecarboxylic acid (E10) (17 mg) as an off-white solid. δH (DMSO-d6, 400 MHz): 0.93 (6H, d), 1.11 (3H, t), 1.99 (1H, m), 2.85 (6H, m), 3.38 (2H, m), 3.61 (1H, m), 4.27 (4H, m), 7.40 (1H, m), 7.51 (2H, t), 7.68 (1H, d), 8.31 (1H, dd), 8.46 (1H, d), 13.04 (1H, br s). MS (ES): C27H30N4O2S requires 474. found 475.2 (M+H+).
WORKUP
后处理
- customThe solvent was removed in vacuo
- dissolutionThe residue was dissolved in THF
- filtrationfiltered
- customThe filtrate was purified by Mass Directed AutoPrep