Cesium carbonate → {6-[4-Isopropyl-2-(4-trifluoromethyl-phenyl)-thiazol-5-ylmethoxy]-benzo[b]thiophen-3-yl}-acetic acid

HRID 490766Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 490766
Cl[CH2:2][C:3]1[S:7][C:6]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)=[N:5][C:4]=1[CH:18]([CH3:20])[CH3:19].C([O:23][C:24](=[O:36])[CH2:25][C:26]1[C:27]2[CH:34]=[CH:33][C:32]([OH:35])=[CH:31][C:28]=2[S:29][CH:30]=1)C.C([O-])([O-])=O.[Cs+].[Cs+].[OH-].[Na+]>C(#N)C.C(O)C>[CH:18]([C:4]1[N:5]=[C:6]([C:8]2[CH:13]=[CH:12][C:11]([C:14]([F:17])([F:16])[F:15])=[CH:10][CH:9]=2)[S:7][C:3]=1[CH2:2][O:35][C:32]1[CH:33]=[CH:34][C:27]2[C:26]([CH2:25][C:24]([OH:36])=[O:23])=[CH:30][S:29][C:28]=2[CH:31]=1)([CH3:20])[CH3:19]

Komponenten

7

Versuchsvorschrift

To a solution of 5-chloromethyl-4-isopropyl-2-(4-trifluoromethyl-phenyl)-thiazole (100 mg, 0.31 mmol) and (6-Hydroxy-benzo[b]thiophen-3-yl)-acetic acid ethyl ester (75 mg, 0.31 mmol) in acetonitrile (3 mL) is added Cs2CO3 (200 mg, 0.62 mmol). The mixture is stirred at room temperature overnight, ethanol (1 mL) is added, followed by NaOH (5 N, 1.0 mL). The mixture is heated at 50° C. for 2 hrs, solvent is evaporate, the residue is diluted with water, acidified by 5N HCl and extracted with ethyl acetate. Concentration and reversed phase HPLC purification yields the title product. MS (ES): 490.0 (M+−1).

Aufarbeitung

  1. temperatureThe mixture is heated at 50° C. for 2 hrs
  2. customsolvent is evaporate
  3. additionthe residue is diluted with water
  4. extractionextracted with ethyl acetate
  5. concentrationConcentration
  6. customphase HPLC purification

Quellen und Nachweise

ORD-Eintrag
ord-693ccb0ba6414c359f00c99c86af5c81
Quelldatensatz
uspto-grants-2009_05
Patentnummer
US07528160B2

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