HRID279879

反应详情

EQUATION

反应方程式

HRID 279879 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

161 mg of (±)-6-fluoro-8-amino-2,3-dihydrospiro[4H-1-benzopyran-4,5'-thiazolidine]-2',4'-dione were dissolved in 3.5 ml of pyridine and esterified with 135 mg of undecanoyl chloride. After stirring at room temperature for 6 hours, the majority of the pyridine was removed in vacuo, the residue was extracted with three portions of ethyl acetate and two portions of 1N hydrochloric acid, the organic phases were washed neutral with water and with saturated sodium chloride solution, dried with sodium sulfate and concentrated. The residue was chromatographed on silica gel with chloroform/methanol (19:1). With Rf =0.27 there were eluted 182 mg of material in the form of a resin which yielded, from methanol, (±)-6-fluoro-8-undecylamido-2,3-dihydrospiro[4H-1-benzopyran-4,5'-thiazolidine]-2',4'-dione in the form of colorless crystals of melting point 69°-71° C.

WORKUP

后处理

  1. customthe majority of the pyridine was removed in vacuo
  2. extractionthe residue was extracted with three portions of ethyl acetate and two portions of 1N hydrochloric acid
  3. washthe organic phases were washed neutral with water and with saturated sodium chloride solution
  4. dry with materialdried with sodium sulfate
  5. concentrationconcentrated
  6. customThe residue was chromatographed on silica gel with chloroform/methanol (19:1)
  7. washWith Rf =0.27 there were eluted 182 mg of material in the form of a resin which