HRID1735882

反应详情

EQUATION

反应方程式

HRID 1735882 的结构方程式

AUXILIARIES

试剂、催化剂与溶剂

1

CONDITIONS

反应条件

温度
60 °C

PROCEDURE

实验过程

A mixture of 2-isothiocyano-1,2,3,4-tetrahydronaphthalene (1.92 g, 10.1 mmol), prepared as in Example 10, and aminoacetonitrile hydrochloride (0.94 g, 10.1 mmol) in 1.41 mL of triethylamine was heated at 60° C. for 1 hour. The solvent was evaporated and the residue was purified by flash chromatography (elution: methylene chloride followed by 3% methanol in methylene chloride). The purified residue was recrystallized from ethyl acetate/hexane. The residue (1.06 g) and 44 mL of 0.1N potassium hydroxide was stirred under nitrogen for 15 minutes. The residue was isolated by filtration, washed with water, air dried and then stirred with methylene chloride. Filtration and drying gave 5-amino-1-(1,2,3,4-tetrahydronaphthalen-2-yl)-1,3-dihydroimidazole-2-thione, m.p. 169°-171° C.

WORKUP

后处理

  1. customThe solvent was evaporated
  2. customthe residue was purified by flash chromatography (elution: methylene chloride followed by 3% methanol in methylene chloride)
  3. customThe purified residue was recrystallized from ethyl acetate/hexane
  4. customThe residue was isolated by filtration
  5. washwashed with water, air
  6. customdried
  7. stirringstirred with methylene chloride
  8. filtrationFiltration
  9. customdrying