HRID1177453

反应详情

EQUATION

反应方程式

HRID 1177453 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 2,6-dimethyl-4-(5-(1-phenylcyclopropyl)thiazolo[5,4-b]pyridine-2-yl)benzaldehyde (22.4 mg, 58.3 μmol), azetidine-3-carboxylic acid (29.5 mg, 291 μmol), and acetic acid (26.9 μl, 466 μmol) in 1:1 CH2Cl2/MeOH (2.0 mL) was stirred at 25° C. for 1 h. Sodium cyanoborohydride (6.59 mg, 105 μmol) 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 2 mL DMSO+20 μL trifluoroacetic acid, 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).

WORKUP

后处理

  1. stirringthe resulting mixture was stirred at 25° C. for 15 h
  2. concentrationThe reaction mixture was then concentrated in vacuo
  3. dissolutiondissolved in 2 mL DMSO+20 μL trifluoroacetic acid
  4. filtrationfiltered
  5. custompurified by rpHPLC (10-100% acetonitrile/water+0.1% TFA)