Réaction #1797515

ord-dabb1a89e9dd4857a393e4a8d7cfebce

Équation de réaction

COC(=O)c1ccc(N2CCNC2=O)cc1
Methyl 4-(2-oxoimidazolidin-1-yl)benzoate
CC(C)(C)c1ccc(I)cc1I
iodo-1-tert-butyl-4-iodobenzene
O=P([O-])([O-])[O-].[K+].[K+].[K+]
K3PO4
CNCCNC
N,N′-dimethyl ethylenediamine
COC(=O)c1ccc(N2CCN(c3ccc(C(C)(C)C)cc3)C2=O)cc1
Methyl 4-(3-(4-tert-butylphenyl)-2-oxoimidazolidin-1-yl)benzoate

Solvants

Conditions de réaction

Température
110°CELSIUS
Conditions détaillées
See reaction.notes.procedure_details.

Traitement

  1. 1
    Autrethe solvent was removed in vacuum
  2. 2
    Autrepurified on ISCO system (5% methanol in dichloromethane)
  3. 3
    Autreto give a pure product as a white crystalline (275 mg, 78%)

Mode opératoire

Methyl 4-(2-oxoimidazolidin-1-yl)benzoate (220 mg, 1.0 mmole) was mixed with iodo-1-tert-butyl-4-iodobenzene (260 mg, 1.0 mmol), CuI (38 mg, 0.2 mmol), K3PO4 (426 mg, 2 mmol), N,N′-dimethyl ethylenediamine (17 mg, 0.2 mmol) and 1,4-dioxane (5 ml). The mixture was heated at 110° C. with stirring for 12 hours, and the solvent was removed in vacuum. The residue was suspended in dichloromethane and purified on ISCO system (5% methanol in dichloromethane) to give a pure product as a white crystalline (275 mg, 78%): 1H NMR (400 MHz, CDCl3) δ 8.05 (dd, 2H), 7.70 (dd, 2H), 7.36 (dd, 2H), 7.20 (dd, 2H), 4.02 (s, 4H), 3.90 (s, 3H), 1.30 (s, 9H). MS (ESI) m/z: Calculated: 352.18; Observed: 353.10 (M++1).

Source

DOI: 10.6084/m9.figshare.5104873.v1Brevet: US07790707B2uspto-grants-2010_09