Water → methyl (3R,4R)-4-[3-oxo-3-(6-methoxyquinolin-4-yl)propyl]-1-[prop-2-ynyl]piperidine-3-acetate

HRID 2186397Notes

Reaction equation

HRID 2186397 reaction equation
C(N(CC)CC)C.[O:8]=[C:9]([C:23]1[C:32]2[C:27](=[CH:28][CH:29]=[C:30]([O:33][CH3:34])[CH:31]=2)[N:26]=[CH:25][CH:24]=1)[CH2:10][CH2:11][C@@H:12]1[CH2:17][CH2:16][NH:15][CH2:14][C@@H:13]1[CH2:18][C:19]([O:21][CH3:22])=[O:20].[CH2:35](Br)[C:36]#[CH:37].O>CN(C)C=O>[O:8]=[C:9]([C:23]1[C:32]2[C:27](=[CH:28][CH:29]=[C:30]([O:33][CH3:34])[CH:31]=2)[N:26]=[CH:25][CH:24]=1)[CH2:10][CH2:11][C@@H:12]1[CH2:17][CH2:16][N:15]([CH2:37][C:36]#[CH:35])[CH2:14][C@@H:13]1[CH2:18][C:19]([O:21][CH3:22])=[O:20]

Participants

6

Reactant 4

HCID 962WaterHCID 7842Propargyl bromideHCID 8471TriethylamineHCID 70173611HCID 70173611, compound

Product 1

HCID 86758168methyl (3R,4R)-4-[3-oxo-3-(6-methoxyquinolin-4-yl)propyl]-1-[prop-2-ynyl]piperidine-3-acetate

Reagents, catalysts & solvents 1

HCID 6228DimethylformamideSolvent

Conditions

Temperature
45 °C

Procedure

4.8 cm3 of triethylamine were added with stirring, at a temperature in the region of 20° C. and under an inert atmosphere, to a solution of 5 g of methyl (3R,4R)-4-[3-oxo-3-(6-methoxyquinolin-4-yl)propyl]piperidine-3-acetate in 60 cm3 of dimethylformamide. After stirring for 15 minutes at this temperature, 1.5 cm3 of propargyl bromide were added over approximately 15 minutes and then, after 15 minutes, the mixture was heated at a temperature in the region of 45° C. for 4 hours. After cooling to approximately 20° C., the reaction mixture was poured onto approximately 700 cm3 of water and then the mixture was extracted with 4 times 80 cm3 of diethyl ether. The combined extracts were washed with 3 times 80 cm3 of water, dried, filtered, and concentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C. The evaporation residue was purified by chromatography at atmospheric pressure on a column of silica gel (particle size 20-45 μm; diameter 4 cm; silica volume 500 cm3), elution was carried out with pure ethyl acetate, and 60-cm3 fractions were collected. Fractions 9 to 20 were combined and then concentrated as under the above conditions. 4.3 g of methyl (3R,4R)-4-[3-oxo-3-(6-methoxyquinolin-4-yl)propyl]-1-[prop-2-ynyl]piperidine-3-acetate were obtained in the form of an oil with a yellow color.

Workup

  1. additionwere added over approximately 15 minutes
  2. temperatureAfter cooling to approximately 20° C.
  3. extractionthe mixture was extracted with 4 times 80 cm3 of diethyl ether
  4. washThe combined extracts were washed with 3 times 80 cm3 of water
  5. customdried
  6. filtrationfiltered
  7. concentrationconcentrated under reduced pressure (5 kPa) at a temperature in the region of 40° C
  8. customThe evaporation residue was purified by chromatography at atmospheric pressure on a column of silica gel (particle size 20-45 μm; diameter 4 cm; silica volume 500 cm3), elution
  9. customwere collected
  10. concentrationconcentrated as under the above conditions

Sources & evidence

ORD record
ord-e3a79ca7e9e8466baebc49c40399869c
Source dataset
uspto-grants-2002_06
Patent number
US06403610B1

Reaction notes

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