HRID712324

反应详情

EQUATION

反应方程式

HRID 712324 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

2

PROCEDURE

实验过程

Ethyl 1-[5-[2-(3-ethyl-5-methyl-2-oxo-1,3,5-triazinan-1-yl)-7-(iodomethyl)-1,3-benzothiazol-5-yl]pyrimidin-2-yl]-4-methyl-piperidine-4-carboxylate (160 mg, 0.241 mmol) and 2-methoxyethanol (95 μL, 1.21 mmol) were dissolved in THF (10 mL). Sodium hydride (96 mg, 2.41 mmol) was added portion-wise and the mixture stirred under argon at rt for 1 h. The mixture was then diluted with EtOAc (50 mL), carefully quenched with saturated aqueous NH4Cl, washed with water, brine and separated. The organic fraction was dried (Na2SO4), concentrated under reduced pressure and the resulting solid residue purified by flash column chromatography (40 g GraceResolv, silica cartridge) eluting with 50-100% EtOAc/heptane to afford the desired compound (86 mg, 58%) as a colourless resin. MS: 612.16 [M+H]+.

WORKUP

后处理

  1. customcarefully quenched with saturated aqueous NH4Cl
  2. washwashed with water, brine
  3. customseparated
  4. dry with materialThe organic fraction was dried (Na2SO4)
  5. concentrationconcentrated under reduced pressure
  6. customthe resulting solid residue purified by flash column chromatography (40 g GraceResolv, silica cartridge)
  7. washeluting with 50-100% EtOAc/heptane