Reaktion #80449

Reaktionsgleichung

dimethylformamide

2-iodo-5-[2-{3-pyridyl}ethenyl]furan

N-hydroxy-N-(butyn-2-yl)urea

NH4OH

→

title compound

Ausbeute 37.9%

N-[3-(5-{2-[3-pyridyl]ethenyl}fur-2-yl)-1-methyl-2-propynyl]-N-hydroxyurea

Ausbeute 37.9%

Lösungsmittel

diethylamine

Reaktionsbedingungen

Aufarbeitung

1. 1
   Extraktionthe mixture extracted thoroughly with CH2Cl2
2. 2
   WaschenThe combined organic layer was washed with brine
3. 3
   Trocknendried (MgSO4)
4. 4
   Sonstigeevaporated under reduced pressure
5. 5
   SonstigeThe resulting residue was purified by column chromatography on silica gel eluting with 5% MeOH
6. 6
   SonstigeCH2Cl2 to afford an off-white solid
7. 7
   SonstigeRecrystallization from ethyl acetate-hexanes

Vorschrift

To a stirred solution of 2-iodo-5-[2-{3-pyridyl}ethenyl]furan (1.4 g, 4.7 mmol), prepared as in step 5, and N-hydroxy-N-(butyn-2-yl)urea (0.64 g, 5 mmol), prepared as in step 2, in diethylamine (10 mL) was added dimethylformamide (1 mL), triphenylphosphine (0.026 g, 0.1 mmol), cuprous iodide (5 mg, 25 mmol) and bis(acetonitrile)palladium(II) chloride (13 mg, 50 mmol). The mixture was stirred overnight at ambient temperature. Aqueous NH4OH was added and the mixture extracted thoroughly with CH2Cl2. The combined organic layer was washed with brine, dried (MgSO4) and evaporated under reduced pressure. The resulting residue was purified by column chromatography on silica gel eluting with 5% MeOH--CH2Cl2 to afford an off-white solid. Recrystallization from ethyl acetate-hexanes gave 530 mg of the title compound. m.p. 166° C. 1H NMR (DMSO-d6, 300 MHz) δ1.38 (d, J=7 Hz, 3H), 5.19 (q, J=7 Hz, 1H), 6.61 (bs, 2H), 6.82 (d, J=3 Hz, 1H), 6.82 (d, J=3 Hz, 1H), 7.09 (d, J=16 Hz, 1H), 7.25 (d, J=16 Hz, 1H), 7.39 (m, 1H), 7.77 (m, 1H), 8.03 (m, 1H), 8.45 (m, 1H), 8.77 (m, 1H), 9.43 (s, 1H). MS (DCI/NH3) m/e 298 (M+H)+. Anal calcd for C16H15N3O3 : C, 64.63; H, 5.08; N, 14.13. Found: C, 64.01; H, 5.09; N, 14.06.

Quelle