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Potassium Carbonate → 1-(3-(Trifluoromethyl)pyridin-2-YL)piperidin-4-one

HRID 1246720
Notes
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Reaction equation

HRID 1246720 reaction equation
Cl[C:2]1[C:7]([C:8]([F:11])([F:10])[F:9])=[CH:6][CH:5]=[CH:4][N:3]=1.C([O-])([O-])=O.[K+].[K+].O1[C:22]2([CH2:27][CH2:26][NH:25][CH2:24][CH2:23]2)[O:21]CC1>CS(C)=O.C(OCC)C>[F:9][C:8]([F:11])([F:10])[C:7]1[C:2]([N:25]2[CH2:26][CH2:27][C:22](=[O:21])[CH2:23][CH2:24]2)=[N:3][CH:4]=[CH:5][CH:6]=1
ParticipantsConditionsProcedureWorkupSources & evidenceReaction notes

Participants

6

Reactant 3

HCID 11430Potassium CarbonateHCID 674351,4-Dioxa-8-azaspiro(4.5)decane3×HCID 5898332-Chloro-3-(trifluoromethyl)pyridine

Product 1

HCID 219047511-(3-(Trifluoromethyl)pyridin-2-YL)piperidin-4-one

Reagents, catalysts & solvents 2

HCID 679Dimethyl SulfoxideSolvent
HCID 3283
Diethyl Ether
Solvent

Conditions

Temperature
100 °C

Procedure

2-Chloro-3-(trifluoromethyl)pyridine (11.92 g, 65.7 mmol)), K2CO3(19.10 g, 138 mmol), and 1,4-dioxa-8-azaspiro[4.5]decane (8.85 mL, 69.0 mmol) were combined in DMSO (65 mL) and stirred at 100° C. for 3 hours. The mixture was treated with additional 1,4-dioxa-8-azaspiro[4.5]decane (2.0 mL, 16 mmol), stirred for 2 hours, treated with additional 1,4-dioxa-8-azaspiro[4.5]decane (1.0 mL, 7.8 mmol), and stirred for 1 hour. The mixture was diluted with diethyl ether (200 mL), washed with water (250 mL), washed with brine (100 mL), dried (Na2SO4), filtered, and the filtrate was concentrated under reduced pressure. The residue was dissolved in concentrated HCl (25 mL), stirred for 3 hours, basified with concentrated NH4OH, extracted with CH2Cl2, and the phases separated. The organic phase was dried (Na2SO4), filtered, and the filtrate concentrated under reduced pressure. The residue was purified via flash chromatography (20% to 40% diethyl ether/hexanes) to provide the title compound.

Workup

  1. stirringstirred for 2 hours
  2. stirringstirred for 1 hour
  3. washwashed with water (250 mL)
  4. washwashed with brine (100 mL)
  5. dry with materialdried (Na2SO4)
  6. filtrationfiltered
  7. concentrationthe filtrate was concentrated under reduced pressure
  8. dissolutionThe residue was dissolved in concentrated HCl (25 mL)
  9. stirringstirred for 3 hours
  10. extractionextracted with CH2Cl2
  11. customthe phases separated
  12. dry with materialThe organic phase was dried (Na2SO4)
  13. filtrationfiltered
  14. concentrationthe filtrate concentrated under reduced pressure
  15. customThe residue was purified via flash chromatography (20% to 40% diethyl ether/hexanes)

Sources & evidence

ORD record
ord-631430483e924be19e134610c3030daa
Source dataset
uspto-grants-2006_10
DOI
10.6084/m9.figshare.5104873.v1
Patent number
US07129235B2

Reaction notes

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On this pageParticipantsConditionsProcedureWorkupSources & evidenceReaction notes