Реакция #2161255

ord-721dd9feeb6843cf82e5f636be6397c1

Уравнение реакции

O=C=Nc1ccc(OC(F)(F)F)cc1
4-(trifluoromethoxy)phenyl isocyanate
CCOC(=O)c1nc(N)cn1C
ethyl 4-amino-1-methyl-1H-imidazole-2-carboxylate
CCOC(=O)c1nc(NC(=O)Nc2ccc(OC(F)(F)F)cc2)cn1C
Ethyl 1-methyl-4-[({[4-(trifluoromethoxy)phenyl]amino}carbonyl)amino]-1H-imidazole-2-carboxylate

Растворители

Условия реакции

Подробные условия
See reaction.notes.procedure_details.

Обработка

  1. 1
    Другоеsynthesis in analogy to Example 4A step 3
  2. 2
    ФильтрацияThe reaction mixture is filtered
  3. 3
    Концентрированиеthe filtrate is concentrated in vacuo
  4. 4
    Другоеpurified chromatographically

Методика

Under argon, 1.46 g (7.21 mmol) of 4-(trifluoromethoxy)phenyl isocyanate are added to 1.22 g (3.61 mmol) of ethyl 4-amino-1-methyl-1H-imidazole-2-carboxylate (synthesis in analogy to Example 4A step 3, or also according to Tetrahedron Lett. 2003, 44, 1607 and the literature cited therein) in 50 ml of THF, and the mixture is stirred at room temperature overnight. The reaction mixture is filtered and the filtrate is concentrated in vacuo and purified chromatographically.

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: US07919489B2uspto-grants-2011_04