Potassium Carbonate → HCID 22558061, compound

HRID 1937663Notes

Reaction equation

HRID 1937663 reaction equation
[NH:1]1[CH2:6][CH2:5][CH:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]1.Cl[CH2:13][C:14]1[CH:19]=[CH:18][N:17]=[C:16]([C:20]2[CH:25]=[C:24]([O:26][CH3:27])[C:23]([O:28][CH3:29])=[C:22]([O:30][CH3:31])[CH:21]=2)[CH:15]=1.C(=O)([O-])[O-].[K+].[K+]>C(#N)C>[CH3:27][O:26][C:24]1[CH:25]=[C:20]([C:16]2[CH:15]=[C:14]([CH2:13][N:1]3[CH2:6][CH2:5][CH:4]([C:7]([O:9][CH2:10][CH3:11])=[O:8])[CH2:3][CH2:2]3)[CH:19]=[CH:18][N:17]=2)[CH:21]=[C:22]([O:30][CH3:31])[C:23]=1[O:28][CH3:29]

Participants

5

Procedure

To a solution of ethyl piperidine-4-carboxylate (514 mg) and 4-chloromethyl-2-(3,4,5-trimethoxyphenyl)pyridine (969 mg) in acetonitrile (20 mL) was added potassium carbonate (452 mg). The mixture was stirred at room temperature for 4 hours and evaporated. The residual oil was subjected to a column of silica gel and eluted using hexane-ethyl acetate (2:1) and then chloroform-methanol (40:1). Fractions containing the product were collected and evaporated to give the title compound as white prisms.

Workup

  1. customevaporated
  2. washeluted
  3. additionFractions containing the product
  4. customwere collected
  5. customevaporated

Sources & evidence

ORD record
ord-2ef9ddb8a5274dcaac3fdc7ca321dfd8
Source dataset
uspto-grants-2002_05
Patent number
US06395753B1

Reaction notes

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