반응 #48480

ord-035ea214a9664fb0b0a198a21ab33606

반응 조건

상세 조건
See reaction.notes.procedure_details.

후처리

  1. 1
    workup.WAITThe resulting suspension is left
  2. 2
    workup.ADDITIONis then added dropwise
  3. 3
    workup.WAITthe suspension is then left
  4. 4
    workup.STIRRINGunder stirring for 4 h
  5. 5
    workup.ADDITIONis added to the reaction mixture
  6. 6
    여과filtration
  7. 7
    기타to remove the remains of indole-3-carboxylic acid in excess, the resulting phases
  8. 8
    기타are separated
  9. 9
    건조The organic phase is dried over magnesium sulphate
  10. 10
    기타evaporated to dryness

실험 절차

Indole-3-carboxylic acid (6.43 gr, 39.9 mmol) is added in portions to a solution of 5.33 mL (37.7 mmol) of trifluoroacetic anhydride in dichloromethane (172 mL) and under nitrogen atmosphere. The resulting suspension is left under stirring for 30 minutes. 7-hydroxy-9-methoxycarbonylmethyl-9-aza-bicyclo[3.3.1]nonan-3-carboxylic acid methyl ester (6 gr, 22.1 mmol) dissolved in dichloromethane (15 mL) is then added dropwise. Next, a catalytic amount of DMAP is added, and the suspension is then left under stirring for 4 h. Following that time, and once the limiting starting product has been used up as shown by thin-layer chromatography (dichloromethane/methanol/ammonia 90:10:1, which reveals potassium permanganate), water (50 mL) is added to the reaction mixture and the mixture is basified with a saturated aqueous solution of sodium bicarbonate. Following filtration to remove the remains of indole-3-carboxylic acid in excess, the resulting phases are separated. The organic phase is dried over magnesium sulphate and evaporated to dryness, to give 7-(1H-Indole-3-carbonyloxy)-9-methoxycarbonylmethyl-9-aza-bicyclo[3.3.1]nonane-3-carboxylic acid methyl ester as a white solid (8.20 gr, 89%) that can be used directly in the following synthesis step.

출처

DOI: 10.6084/m9.figshare.5104873.v1특허: US07745628B2uspto-grants-2010_06