HRID1421466

反应详情

EQUATION

反应方程式

HRID 1421466 的结构方程式

CONDITIONS

反应条件

温度
15 °C

PROCEDURE

实验过程

A solution of 4.0 grams (0.011 mole) of 3-(3-amino-4-chloro-6-fluoro-2-methoxyphenyl)-1-methyl-6-trifluoromethyl-2,4-(1H,3H)-pyrimidinedione in 25 mL (0.300 mole) of concentrated hydrochloric acid was stirred and cooled in an ice bath. During a 15 minute period, 1.9 grams (0.013 mole) of sodium nitrite was added dropwise at a rate to maintain the reaction temperature at 15° C. Upon completion of addition, the mixture was stirred for 20 minutes and then poured into 15.0 grams (0.090 mole) of potassium iodide. The reaction mixture was stirred for 30 minutes and then filtered. The filter cake was thoroughly washed with distilled water and then taken up in 150 mL of ethyl acetate. The resulting solution was dried with sodium sulfate and filtered. The filtrate was concentrated under reduced pressure to yield a brown solid. The solid was subjected to column chromatography on silica gel. Elution was accomplished using 5:1 heptane and ethyl acetate. The product-containing fractions were combined and concentrated under reduced pressure, yielding 3.0 grams of title compound. The NMR spectrum was consistent with the proposed structure.

WORKUP

后处理

  1. temperaturecooled in an ice bath
  2. additionUpon completion of addition
  3. stirringThe reaction mixture was stirred for 30 minutes
  4. filtrationfiltered
  5. washThe filter cake was thoroughly washed with distilled water
  6. dry with materialThe resulting solution was dried with sodium sulfate
  7. filtrationfiltered
  8. concentrationThe filtrate was concentrated under reduced pressure
  9. customto yield a brown solid
  10. washElution
  11. concentrationconcentrated under reduced pressure