HRID1177472

反应详情

EQUATION

反应方程式

HRID 1177472 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
25 °C

PROCEDURE

实验过程

A mixture of 2-methyl-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)benzaldehyde (22.6 mg, 0.061 mmol), azetidine-3-carboxylic acid (31 mg, 0.305 mmol), and acetic acid (28 μL, 0.488 mmol) in 1:1 CH2Cl2/MeOH (2.0 mL) was stirred at 25° C. for 1 h. Sodium cyanoborohydride (6.9 mg, 0.110 mmol) was then added, and the resulting mixture was stirred at 25° C. for 16 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-methyl-4-(5-(1-phenyl-cyclopropyl)thiazolo[5,4-b]pyridine-2-yl)phenyl)methyl)azetidine-3-carboxylic acid as a white solid. MS (ESI) m/z: Calculated: 455.2; Observed: 456.1 (M++1).

WORKUP

后处理

  1. stirringthe resulting mixture was stirred at 25° C. for 16 h
  2. concentrationThe reaction mixture was then concentrated in vacuo
  3. dissolutiondissolved in DMSO (2 mL)+trifluoroacetic acid (20 μL)
  4. filtrationfiltered
  5. custompurified by rpHPLC (10-100% acetonitrile/water+0.1% TFA)