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
CONDITIONS
反应条件
- 温度
- 25 °C
PROCEDURE
实验过程
A mixture of 2,6-dimethyl-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)benzaldehyde (22.4 mg, 0.058 mmol), azetidine-3-carboxylic acid (29.5 mg, 0.29 mmol), and acetic acid (26.9 μl, 0.466 mmol) in 1:1 CH2Cl2/MeOH (2.0 mL) was stirred at 25° C. for 1 h. Sodium cyanoborohydride (6.59 mg, 0.105 mmol) was then added, and the resulting mixture was stirred at 25° C. for 15 h. The reaction mixture was then concentrated in vacuo, dissolved in DMSO (2 mL)+trifluoroacetic acid (20 μL), filtered, and purified by rpHPLC (10-100% acetonitrile/water+0.1% TFA) to provide 1-((2,6-dimethyl-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)phenyl)methyl)azetidine-3-carboxylic acid as a light yellow solid. MS (ESI) m/z: Calculated: 469.2; Observed: 470.1 (M++1). (2,6-
WORKUP
后处理
- stirringthe resulting mixture was stirred at 25° C. for 15 h
- concentrationThe reaction mixture was then concentrated in vacuo
- dissolutiondissolved in DMSO (2 mL)+trifluoroacetic acid (20 μL)
- filtrationfiltered
- custompurified by rpHPLC (10-100% acetonitrile/water+0.1% TFA)