Potassium Carbonate → HCID 57861236, compound

HRID 1518088Notes

Reaction equation

HRID 1518088 reaction equation
Cl[C:2]1[C:11]([CH:12]=[O:13])=[CH:10][C:9]2[C:4](=[CH:5][C:6]([F:15])=[C:7]([F:14])[CH:8]=2)[N:3]=1.[CH2:16]([O:23][CH2:24][CH2:25][C@H:26]1[CH2:31][CH2:30][C@H:29]([C@H:32]2[CH2:36][CH2:35][CH2:34][NH:33]2)[CH2:28][CH2:27]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1.C(=O)([O-])[O-].[K+].[K+]>C1(C)C=CC=CC=1.O.Cl.C(OCC)(=O)C>[CH2:16]([O:23][CH2:24][CH2:25][CH:26]1[CH2:31][CH2:30][CH:29]([C@H:32]2[CH2:36][CH2:35][CH2:34][N:33]2[C:2]2[C:11]([CH:12]=[O:13])=[CH:10][C:9]3[C:4](=[CH:5][C:6]([F:15])=[C:7]([F:14])[CH:8]=3)[N:3]=2)[CH2:28][CH2:27]1)[C:17]1[CH:22]=[CH:21][CH:20]=[CH:19][CH:18]=1

Participants

8

Procedure

A suspension of 2-chloro-6,7-difluoroquinoline-3-carbaldehyde (8.30 g, 36 mmol), trans-(R)-2-[4-(benzyloxyethyl)cyclohexyl]pyrrolidine (10.5 g, 36 mmol), and potassium carbonate (7.60 g, 55 mmol) in toluene (90 mL) and water (12 mL) is stirred and refluxed for 4 hours. The reaction mixture is cooled to room temperature and then diluted with 1N HCl aq. and ethyl acetate. The organic layer is washed with sat. NaHCO3 aq., brine, dried over magnesium sulfate, filtered and concentrated to give 2-((R)-2-{4-[2-(benzyloxy)ethyl]cyclohexyl}pyrrolidin-1-yl)-6,7-difluoroquinoline-3-carbaldehyde as yellow syrup, which is used without further purification.

Workup

  1. temperaturerefluxed for 4 hours
  2. washThe organic layer is washed with sat. NaHCO3 aq., brine
  3. dry with materialdried over magnesium sulfate
  4. filtrationfiltered
  5. concentrationconcentrated

Sources & evidence

ORD record
ord-3fcfd2d8d48c4c039dd15d796cda812e
Source dataset
uspto-grants-2012_07
Patent number
US08232403B2

Reaction notes

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