Reaktion #167248

ord-c1397169756649398543cfcb13ccec47

Reaktionsgleichung

Cc1ccncc1N1CCNC1=O
1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one
Brc1cccs1
2-bromo-thiophene
N[C@@H]1CCCC[C@H]1N
trans-1,2-diamino cyclohexane
O=C([O-])[O-].[K+].[K+]
potassium carbonate
Cc1ccncc1N1CCN(c2cccs2)C1=O
product
Ausbeute 109.3%
Cc1ccncc1N1CCN(c2cccs2)C1=O
1-(4-Methyl-pyridin-3-yl)-3-thiophen-2-yl-imidazolidin-2-one
Ausbeute 109.3%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Sonstigeto afford the crude product
  2. 2
    SonstigePurification by column chromatography on silica gel (1% MeOH in DCM)

Vorschrift

Using the same reaction conditions as in Example 14, 1-(4-methyl-pyridin-3-yl)-imidazolidin-2-one (I-14b: 150 mg, 0.847 mmol) was reacted with 2-bromo-thiophene (0.08 mL, 0.847 mmol), 1,4-dioxane (10 mL), copper iodide (16.13 mg, 0.0847 mmol), trans-1,2-diamino cyclohexane (0.03 mL) and potassium carbonate (233 mg, 1.694 mmol) to afford the crude product. Purification by column chromatography on silica gel (1% MeOH in DCM) afforded 240 mg of the product (48.4% yield).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: USRE045173E1uspto-grants-2014_09