HRID1902332

反应详情

EQUATION

反应方程式

HRID 1902332 的结构方程式

PROCEDURE

实验过程

3-(2,2,2-Trifluoroethyl)amino-5-amino-1,2,4-thiadiazole (2.0 g.) and tetrahydropyranyloxyacetamidine hydrochloride (2.0 g.) was added to a solution of sodium ethoxide prepared from sodium (0.46 g.) and alcohol (50 ml.). The resulting mixture was stirred at 20° for 4 hours then heated under reflux for 60 hours. Volatile material was evaporated in vacuo and the residue was shaken with 2 N hydrochloric acid (30 ml.) and ethyl acetate (30 ml.). The aqueous layer was further extracted with ethyl acetate (3×30 ml.) then the pH was adjusted to 10 with 2 N sodium hydroxide. The basified mixture was extracted with ethyl acetate (6×30 ml.) and the combined extracts were dried (MgSO4) and evaporated in vacuo to give the crude product as an oil. It could be purified by fractionation on a silica gel column eluted with ethyl acetate to give 5-[2-(2,2,2-trifluoroethyl)guanidino]-3-hydroxymethyl-1,2,4-thiadiazole, m.p. 123°-125°.

WORKUP

后处理

  1. temperaturethen heated
  2. temperatureunder reflux for 60 hours
  3. customVolatile material was evaporated in vacuo
  4. stirringthe residue was shaken with 2 N hydrochloric acid (30 ml.) and ethyl acetate (30 ml.)
  5. extractionThe aqueous layer was further extracted with ethyl acetate (3×30 ml.)
  6. extractionThe basified mixture was extracted with ethyl acetate (6×30 ml.)
  7. dry with materialthe combined extracts were dried (MgSO4)
  8. customevaporated in vacuo
  9. customto give the crude product as an oil
  10. customIt could be purified by fractionation on a silica gel column
  11. washeluted with ethyl acetate