Potassium Carbonate → 2-(Morpholine-4-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-one

HRID 1873514Notes

Reaction equation

HRID 1873514 reaction equation
FC(F)(F)C(O)=O.[CH2:8]1[CH:12]2[CH2:13][C:14](=[O:16])[CH2:15][CH:11]2[CH2:10][NH:9]1.C(=O)([O-])[O-].[K+].[K+].[N:23]1([C:29](Cl)=[O:30])[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1>C(#N)C>[N:23]1([C:29]([N:9]2[CH2:10][CH:11]3[CH2:15][C:14](=[O:16])[CH2:13][CH:12]3[CH2:8]2)=[O:30])[CH2:28][CH2:27][O:26][CH2:25][CH2:24]1

Participants

5

Procedure

Hexahydro-cyclopenta[c]pyrrol-5-one trifluoroacetate 1f (574 mg, 2.4 mmol) was dissolved in 20 mL of acetonitrile with stirring followed by addition of potassium carbonate (0.397 g, 2.88 mmol), and morpholine-4-carbonyl chloride (0.323 mL, 2.64 mmol) upon cooling by an ice-water bath. The reaction mixture was reacted overnight at the same temperature. The mixture was concentrated under reduced pressure and diluted with 50 mL of water. The mixture was extracted with ethyl acetate (50 mL×3). The combined organic extracts were washed with 50 mL of saturated brine, dried over anhydrous magnesium sulfate, filtered and concentrated under reduced pressure. The resulting residue was purified by silica gel column chromatography to obtain the title compound 2-(morpholine-4-carbonyl)-hexahydro-cyclopenta[c]pyrrol-5-one 7a (0.572 g, yield 77.3%) as a colorless oil.

Workup

  1. temperatureupon cooling by an ice-water bath
  2. customThe reaction mixture was reacted overnight at the same temperature
  3. concentrationThe mixture was concentrated under reduced pressure
  4. additiondiluted with 50 mL of water
  5. extractionThe mixture was extracted with ethyl acetate (50 mL×3)
  6. washThe combined organic extracts were washed with 50 mL of saturated brine
  7. dry with materialdried over anhydrous magnesium sulfate
  8. filtrationfiltered
  9. concentrationconcentrated under reduced pressure
  10. customThe resulting residue was purified by silica gel column chromatography

Sources & evidence

ORD record
ord-74ce20201ada41a4b1870fc0b1b3e43b
Source dataset
uspto-grants-2012_11
Patent number
US08304411B2

Reaction notes

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