Reacción #9340

ord-aab96c42632a4a4890d68c2d0cb345b0

Ecuación de reacción

O=C([O-])O.[Na+]
NaHCO3
N#CC1=C(C#N)C(=O)C(Cl)=C(Cl)C1=O
DDQ
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2OCc1ccc(OC)cc1
15-5
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2OCc1ccc(OC)cc1
(Z)-7-{(1R,2S,3R)-3-Hydroxy-2-[1-(4-methoxy-benzyloxy)-indan-5-yl]-5-oxo-cyclopentyl}-hept-5-enoic acid methyl ester
CC(Cl)Cl
dichloroethane
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2=O
15-8
Rendimiento 64.3%
COC(=O)CCC/C=C\C[C@H]1C(=O)C[C@@H](O)[C@@H]1c1ccc2c(c1)CCC2=O
(Z)-7-[(1R,2S,3R)-3-Hydroxy-5-oxo-2-(1-oxo-indan-5-yl)-cyclopentyl]-hept-5-enoic acid methyl ester
Rendimiento 64.3%

Condiciones de reacción

Condiciones detalladas
See reaction.notes.procedure_details.

Tratamiento posterior

  1. 1
    Extracciónthe resulting mixture was extracted with dichloromethane (3×20 mL)
  2. 2
    LavadoThe combined dichloromethane solution was washed with brine
  3. 3
    Secadowas dried (Na2SO4)
  4. 4
    Filtraciónfiltered
  5. 5
    Otroevaporated
  6. 6
    OtroPurification of the residue by flash chromatography on silica gel (60% ethyl acetate/hexanes)

Procedimiento

DDQ (10 mg, 0.041 mmol) was added to a mixture of 15-5 (11 mg, 0.021 mmol) in dichloromethane (0.5 mL)/water (25 μL). After 1 h, dichloroethane (0.5 mL) was added and the reaction was stirred overnight. Saturated NaHCO3 solution was added and the resulting mixture was extracted with dichloromethane (3×20 mL). The combined dichloromethane solution was washed with brine and then was dried (Na2SO4), filtered and evaporated. Purification of the residue by flash chromatography on silica gel (60% ethyl acetate/hexanes) gave 15-8 (5 mg, 59%).

Fuente

DOI: 10.6084/m9.figshare.5104873.v1Patente: US07091231B2uspto-grants-2006_08