Potassium Carbonate → 4-[4-(Diethoxy-phosphorylmethyl)-piperazin-1-ylmethyl]-benzoic acid

HRID 48936

Reaktionsgleichung

Reaktionsgleichung von HRID 48936
[N:1]1([CH2:7][C:8]2[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[CH:10][CH:9]=2)[CH2:6][CH2:5][NH:4][CH2:3][CH2:2]1.[CH2:17]([O:19][P:20]([CH2:25]Cl)(=[O:24])[O:21][CH2:22][CH3:23])[CH3:18].C(=O)([O-])[O-].[K+].[K+]>C(O)C.[Cl-].[Na+].O>[CH2:17]([O:19][P:20]([CH2:25][N:4]1[CH2:5][CH2:6][N:1]([CH2:7][C:8]2[CH:16]=[CH:15][C:11]([C:12]([OH:14])=[O:13])=[CH:10][CH:9]=2)[CH2:2][CH2:3]1)([O:21][CH2:22][CH3:23])=[O:24])[CH3:18]

Komponenten

6

Versuchsvorschrift

To a solution of 4-Piperazin-1-ylmethyl-benzoic acid (4c) and chloromethyl-phosphonic acid diethyl ester (4d) in ethanol was added potassium carbonate. The resulting reaction mixture was refluxed, then cooled to room temperature, diluted with brine, acidified to pH˜4, and extracted with EtOAc until the aqueous layer showed little or no evidence of product by HPLC. The combined organics were dried over MgSO4 and concentrated on rotary evaporator. The desired product was purified by silica gel flash chromatography.

Aufarbeitung

  1. customThe resulting reaction mixture
  2. temperaturewas refluxed
  3. extractionextracted with EtOAc until the aqueous layer
  4. dry with materialThe combined organics were dried over MgSO4
  5. concentrationconcentrated on rotary evaporator
  6. customThe desired product was purified by silica gel flash chromatography

Quellen und Nachweise

ORD-Eintrag
ord-ed6d76fa55dd42c390a02af3e2ddcee4
Quelldatensatz
uspto-grants-2004_03
Patentnummer
US06706699B2

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