HRID2186604

反应详情

EQUATION

反应方程式

HRID 2186604 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

PROCEDURE

实验过程

Methyl 4-4-(2-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate: 105 mg (0.424 mmol) of methyl 4-(aminothioxomethyl)-5-methylthiothiophene-2-carboxylate (Maybridge Chemical Co. LTD., Cornwall, U.K.) was dissolved in 5 mL of reagent grade acetone. 2-Bromo-2′-methoxy acetophenone (0.467 mmol; 110 mg) was added and the solution was allowed to reflux for 3 h. The solution was allowed to cool and the solution concentrated. The crude product was dissolved in 100 mL of CH2Cl2 and washed one time with 50 mL of 1N NaOH. The organic layer was obtained, dried over sodium sulfate, concentrated and purified on a 1 mm silica plate eluting with 20% ethyl acetate/hexane to afford 160 mg (95% yield) of methyl 4-[4-(2-methoxyphenyl)(1,3-thiazol-2-yl)]-5-methylthiothiophene-2-carboxylate.

WORKUP

后处理

  1. temperatureto reflux for 3 h
  2. temperatureto cool
  3. concentrationthe solution concentrated
  4. dissolutionThe crude product was dissolved in 100 mL of CH2Cl2
  5. washwashed one time with 50 mL of 1N NaOH
  6. customThe organic layer was obtained
  7. dry with materialdried over sodium sulfate
  8. concentrationconcentrated
  9. custompurified on a 1 mm silica plate
  10. washeluting with 20% ethyl acetate/hexane