반응 #167245

ord-b01412db9d4540568ef3375a4040f69f

반응 방정식

Cc1ccncc1N1CCNC1=O
1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one
N#Cc1ccc(Br)cc1
4-bromo-benzonitrile
N[C@@H]1CCCC[C@H]1N
trans-1,2-diamino cyclohexane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccncc1N1CCN(c2ccc(C#N)cc2)C1=O
product
수율 64.2%
Cc1ccncc1N1CCN(c2ccc(C#N)cc2)C1=O
4-[3-(4-Methyl-pyridin-3-yl)-2-oxo-imidazolidin-1-yl]-benzonitrile
수율 64.2%

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    기타to afford the crude product
  2. 2
    기타Purification by column chromatography on silica gel (5% MeOH in DCM)

실험 절차

Using the same reaction conditions as in Example 14, 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 150 mg, 0.8465 mmol) was reacted with 4-bromo-benzonitrile (154 mg, 0.84650 mmol), 1,4-dioxane (50 mL), copper iodide (16 mg, 0.084650 mmol), trans-1,2-diamino cyclohexane (29 mg, 0.2539 mmol) and potassium carbonate (468 mg, 3.3860 mmol) to afford the crude product. Purification by column chromatography on silica gel (5% MeOH in DCM) afforded 151 mg of the product (64.2% yield).

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: USRE045173E1uspto-grants-2014_09