HRID479701

反应详情

EQUATION

反应方程式

HRID 479701 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
85 °C

PROCEDURE

实验过程

To a stirred suspension of 2-bromothiazole-4-carboxylic acid (5.13 g, 2 mmol) in anhydrous CH3CN (40 ml) at RT, under N2, TEA (3.80 ml, 27 mmol) and (PhO)2PON3 (5.90 ml, 27 mmol) were added. The resulting solution was heated to 85° C. Upon reaching 85° C., a solution of 6-(piperidylmethyl)-2-pyridylamine (4.74 g, 25 mmol) in anhydrous CH3CN (60 ml) was added. The reaction was maintained at this temperature for 2.25 h. After cooling to RT the mixture was diluted with CH2Cl2 (50 ml) then washed with a saturated solution of NH4Cl(aq) (40 ml). The organic layer was separated, dried over MgSO4, filtered and concentrated under reduced pressure. The residue was purified by flash chromatography on silica gel (3:1/2:1/1:1, EtOAc:acetone) to yield the title compound as a pale yellow solid. MS m/z: 396 (M+H), 398 (M+3). Calc'd for C15H18BrN50S: 395.04.

WORKUP

后处理

  1. customUpon reaching 85° C.
  2. temperatureThe reaction was maintained at this temperature for 2.25 h
  3. temperatureAfter cooling to RT the mixture
  4. washthen washed with a saturated solution of NH4Cl(aq) (40 ml)
  5. customThe organic layer was separated
  6. dry with materialdried over MgSO4
  7. filtrationfiltered
  8. concentrationconcentrated under reduced pressure
  9. customThe residue was purified by flash chromatography on silica gel (3:1/2:1/1:1, EtOAc:acetone)