HRID1889112

反应详情

EQUATION

反应方程式

HRID 1889112 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
110 °C

PROCEDURE

实验过程

A solution of 4-[(2,4-dichloro-3-fluorophenyl)carbonyl]-2-piperazinone (I37)(250 mg, 0.859 mmol) in dry dichloromethane (DCM) (2147 μl) was stirred at room temperature under an atmosphere of argon. Triethyloxonium tetrafluoroborate (179 mg, 0.945 mmol) was added to the stirred solution and the solution was stirred for 2 hours. 5-methyl-1,3-thiazole-4-carbohydrazide (I123) (162 mg, 1.031 mmol) was then added and the resulting solution was stirred for 65 hours (over the weekend), during which time the solvent evaporated. The residue was redissolved in 1-butanol (2147 p1) and the resulting mixture was heated to 110° C. for 3 hours. The solution was allowed to cool to room temperature before being concentrated under reduced pressure to give a yellow coloured oil. The oil was redissolved in DCM (approx. 30 ml) and the organics were subsequently washed with NaHCO3 (sat. aqueous solution approx. 20 ml) and brine (approx. 20 ml). The organics were dried over MgSO4, filtered and concentrated under reduced pressure to give a yellow coloured oil. The oil was chromatographed [SiO2, 0-10% MeOH in DCM] to give a pale yellow coloured oil. The oil was subsequently further purified using MDAP (formic acid method) to give a white coloured solid of desired material in 68 mg.

WORKUP

后处理

  1. stirringthe resulting solution was stirred for 65 hours (over the weekend), during which time the solvent
  2. customevaporated
  3. dissolutionThe residue was redissolved in 1-butanol (2147 p1)
  4. temperatureto cool to room temperature
  5. concentrationbefore being concentrated under reduced pressure
  6. customto give a yellow coloured oil
  7. washthe organics were subsequently washed with NaHCO3 (sat. aqueous solution approx. 20 ml) and brine (approx. 20 ml)
  8. dry with materialThe organics were dried over MgSO4
  9. filtrationfiltered
  10. concentrationconcentrated under reduced pressure
  11. customto give a yellow coloured oil
  12. customThe oil was chromatographed [SiO2, 0-10% MeOH in DCM]
  13. customto give a pale yellow coloured oil
  14. customThe oil was subsequently further purified
  15. customto give a white coloured solid of desired material in 68 mg