Reacción #1726696

ord-b90f2ad6a69d4d16ad36656f23b82fe7

Ecuación de reacción

O=Cc1ccc(O)cc1
4-Hydroxybenzaldehyde
O=C([O-])[O-].[Cs+].[Cs+]
cesium carbonate
COc1ccc(-c2nnc(C(=O)N3CC(OS(C)(=O)=O)C3)o2)cc1
4B
COc1ccc(-c2nnc(C(=O)N3CC(OS(C)(=O)=O)C3)o2)cc1
1-(5-(4-Methoxyphenyl)-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yl methanesulfonate
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(C=O)cc4)C3)o2)cc1
9A
Rendimiento 62.1%
COc1ccc(-c2nnc(C(=O)N3CC(Oc4ccc(C=O)cc4)C3)o2)cc1
4-(1-(5-(4-methoxyphenyl)-1,3,4-oxadiazole-2-carbonyl)azetidin-3-yloxy)benzaldehyde
Rendimiento 62.1%

Disolventes

Condiciones de reacción

Temperatura
110°CELSIUS
Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Temperaturathen cooled to RT
  2. 2
    FiltraciónThe solids were filtered off
  3. 3
    Otrothe filtrate was evaporated
  4. 4
    workup.ADDITIONThe residue was treated with methanol
  5. 5
    Otrothe solid formed
  6. 6
    Filtraciónwas collected by filtration
  7. 7
    OtroDrying under vacuum

Procedimiento

4-Hydroxybenzaldehyde (1.10 g, 9.17 mmol), cesium carbonate (3.49 g, 10.70 mmol) and 4B (2.70 g, 7.64 mmol) were mixed with DMF (80 mL). The mixture was stirred at 110° C. for 18 h then cooled to RT. The solids were filtered off and the filtrate was evaporated. The residue was treated with methanol and the solid formed was collected by filtration. Drying under vacuum gave 1.8 g (62%) of 9A as a beige solid. 1H NMR (500 MHz, DMSO-d6): δ 3.85 (s, 3H), 4.13 (dd, 1H), 4.57 (dd, 1H), 4.65 (dd, 1H), 5.12 (dd, 1H), 5.29 (m, 1H), 7.10 (d, 2H), 7.16 (d, 2H), 7.90 (d, 2H), 8.00 (d, 2H), 9.90 (s, 1H), MS (APCI+) m/z 380 [M+H]+.

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US08110566B2uspto-grants-2012_02