HRID402951

反应详情

EQUATION

反应方程式

HRID 402951 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

CONDITIONS

反应条件

温度
90 °C

PROCEDURE

实验过程

A mixture of 6-amino-3′,4′,5′,6′-tetrahydro-2′H-[3,4′]bipyridinyl-1′-carboxylic acid tert-butyl ester (971 mg, 3.0063 mmol), 6-bromo-8-iodo-imidazo[1,2-a]pyridine (1 g, 3.6075 mmol), Pd2(dba)3 (138 mg, 0.1503 mmol), XantPhos (174 mg, 0.3006 mmol), and Cs2CO3 (2 g, 6.0126 mmol) were combined in dioxane (20 mL) and the solution was stirred at 90° C. under N2 atmosphere for 5 h at which point the TLC showed little starting material remained. The solution was poured onto water and extracted with ethyl acetate. The combined organic layers were washed with brine, dried over Na2SO4, and concentrated. Purification by column chromatography on silica gel (DCM: MeOH, 60:1 eluent) afforded the desired product as yellow solid (1.15 g, 81%). 1H NMR (300 MHz, CDCl3): δ 8.44 (d, J=1.5 Hz, 1H), 8.20 (d, J=2.1 Hz, 1H), 7.92 (s, 1H), 7.84 (d, J=1.5 Hz, 1H), 7.49 (s, 2H), 7.42 (dd, J=8.4, 2.4 Hz, 1H), 6.84 (d, J=8.4 Hz, 1H), 4.27-4.23 (m, 2H), 2.85-2.77 (m, 2H), 2.68-2.58 (m, 1H), 1.84-1.79 (m, 2H), 1.67-1.57 (m, 2H), 1.48 (s, 9H).

WORKUP

后处理

  1. additionThe solution was poured onto water
  2. extractionextracted with ethyl acetate
  3. washThe combined organic layers were washed with brine
  4. dry with materialdried over Na2SO4
  5. concentrationconcentrated
  6. customPurification by column chromatography on silica gel (DCM: MeOH, 60:1 eluent)