تفاعل #2161255

ord-721dd9feeb6843cf82e5f636be6397c1

معادلة التفاعل

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

المذيبات

ظروف التفاعل

الظروف التفصيلية
See reaction.notes.procedure_details.

المعالجة

  1. 1
    أخرىsynthesis in analogy to Example 4A step 3
  2. 2
    ترشيحThe reaction mixture is filtered
  3. 3
    تركيزthe filtrate is concentrated in vacuo
  4. 4
    أخرىpurified chromatographically

الإجراء التجريبي

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.

المصدر

DOI: 10.6084/m9.figshare.5104873.v1براءة الاختراع: US07919489B2uspto-grants-2011_04