Реакция #167374

ord-fcf2d44959bd4ab98d845d89baf12260

Уравнение реакции

Cc1ccncc1N1CCNC1=O
1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one
FC(F)(F)c1cc(Br)ccn1
4-bromo-2-trifluoromethyl-pyridine
N[C@@H]1CCCC[C@H]1N
trans-1,2-diamino cyclohexane
O=P([O-])([O-])[O-].[K+].[K+].[K+]
potassium phosphate
Cc1ccncc1N1CCN(c2ccnc(C(F)(F)F)c2)C1=O
product
Выход 73.5%
Cc1ccncc1N1CCN(c2ccnc(C(F)(F)F)c2)C1=O
1-(4-Methyl-pyridin-3-yl)-3-(2-trifluoromethyl-pyridin-4-yl)-imidazolidin-2-one
Выход 73.5%

Растворители

Условия реакции

Температура
120°CELSIUS
Подробные условия
See reaction.notes.procedure_details.

Методика

Using the same reaction conditions as in Example 15, 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 150 mg, 0.847 mmol) was reacted with 4-bromo-2-trifluoromethyl-pyridine (229 mg, 1.017 mmol), 1,4-dioxane (10 mL), copper iodide (16.13 mg, 0.0847 mmol), trans-1,2-diamino cyclohexane (29.09 mg, 0.254 mmol) and potassium phosphate (44.89 mg, 2.117 mmol). The resulting mixture was heated to 120° C. for 6 hours. The reaction workup afforded 200 mg of the product (73.52% yield).

Источник

DOI: 10.6084/m9.figshare.5104873.v1Патент: USRE045173E1uspto-grants-2014_09