Ethanol → HCID 66782052, compound

HRID 1096793Notes

Reaction equation

HRID 1096793 reaction equation
Br[CH:2]([CH:7](Br)[C:8]1[CH:9]=[C:10]2[C:15](=[CH:16][CH:17]=1)[N:14]=[CH:13][CH:12]=[C:11]2[C:18]1[CH:23]=[CH:22][N:21]=[CH:20][CH:19]=1)[C:3]([O:5][CH3:6])=[O:4].[OH-].[K+].[CH2:27](O)C>>[N:21]1[CH:22]=[CH:23][C:18]([C:11]2[C:10]3[C:15](=[CH:16][CH:17]=[C:8]([C:7]#[C:2][C:3]([O:5][CH2:6][CH3:27])=[O:4])[CH:9]=3)[N:14]=[CH:13][CH:12]=2)=[CH:19][CH:20]=1

Participants

4

Conditions

Temperature
95 °C

Procedure

A slurry of methyl 2,3-dibromo-3-[4-(4-pyridinyl)-6-quinolinyl]propanoate (4.20 g, 9.33 mmol) in ethanol (120 ml) was treated with solid potassium hydroxide pellets in one portion then heated at 95° C. for 2 hours. The reaction was cooled to room temperature then evaporated under reduced pressure. The resulting residue was diluted with ethanol (90 ml) and concentrated H2SO4 (3 ml) then heated at 95° C. for 3.5 hours. Cooled to room temperature then concentrated under reduced pressure. The resulting wet residue was taken into a minimum of water then made neutral with the addition of saturated aqueous NaHCO3 solution. This solution was extracted with EtOAc and the extracts were dried over anhydrous sodium sulfate, filtered and evaporated under reduced pressure. The resulting residue was purified by silica gel chromatography (EtOAc) to give the title compound (1.68 g, 60%) as a pale yellow solid. MS(ES)+ m/e 303 [M+H]+.

Workup

  1. temperatureThe reaction was cooled to room temperature
  2. customthen evaporated under reduced pressure
  3. additionThe resulting residue was diluted with ethanol (90 ml) and concentrated H2SO4 (3 ml)
  4. temperaturethen heated at 95° C. for 3.5 hours
  5. temperatureCooled to room temperature
  6. concentrationthen concentrated under reduced pressure
  7. additionthen made neutral with the addition of saturated aqueous NaHCO3 solution
  8. extractionThis solution was extracted with EtOAc
  9. dry with materialthe extracts were dried over anhydrous sodium sulfate
  10. filtrationfiltered
  11. customevaporated under reduced pressure
  12. customThe resulting residue was purified by silica gel chromatography (EtOAc)

Sources & evidence

ORD record
ord-5739fb8290f24a678f22bd5f8cd5e938
Source dataset
uspto-grants-2012_03
Patent number
US08138347B2

Reaction notes

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