Dimethyl Sulfoxide → toluene-4-sulfonic acid 4-[6-(3,4-dimethyl-phenylcarbamoyl)-1H-benzoimidazol-2-yl]-3,5-dimethyl-phenyl ester

HRID 1514880Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 1514880
[NH2:1][C:2]1[CH:3]=[C:4]([CH:16]=[CH:17][C:18]=1[NH2:19])[C:5]([NH:7][C:8]1[CH:13]=[CH:12][C:11]([CH3:14])=[C:10]([CH3:15])[CH:9]=1)=[O:6].[CH3:20][C:21]1[CH:28]=[C:27]([O:29]CC(=O)N2CCCC2)[CH:26]=[C:25]([CH3:38])[C:22]=1[CH:23]=O.[OH2:39].C[S:41]([CH3:43])=[O:42]>>[CH3:15][C:10]1[CH:9]=[C:8]([NH:7][C:5]([C:4]2[CH:16]=[CH:17][C:18]3[N:19]=[C:23]([C:22]4[C:25]([CH3:38])=[CH:26][C:27]([O:29][S:41]([C:43]5[CH:17]=[CH:16][C:4]([CH3:5])=[CH:3][CH:2]=5)(=[O:39])=[O:42])=[CH:28][C:21]=4[CH3:20])[NH:1][C:2]=3[CH:3]=2)=[O:6])[CH:13]=[CH:12][C:11]=1[CH3:14]

Komponenten

5

Versuchsvorschrift

To a solution of 3,4-diamino-N-(3,4-dimethyl-phenyl)-benzamide (102 mg) in DMSO (2 mL) were added 2,6-dimethyl-4-(2-oxo-2-pyrrolidin-1-yl-ethoxy)-benzaldehyde (116 mg) and FeCl3 (1.2 mL in 0.02M THF solution). The mixture was stirred in open air at ambient temperature overnight. The mixture was then diluted by water and extracted with EtOAc. The extracts were dried over Na2SO4, filtered and concentrated under reduced pressure. The crude product was purified by column chromatography (SiO2, EtOAc:Hexane=20:80 to 80:10) to give toluene-4-sulfonic acid 4-[6-(3,4-dimethyl-phenylcarbamoyl)-1H-benzoimidazol-2-yl]-3,5-dimethyl-phenyl ester: MS (m/z) 540 (M+1).

Aufarbeitung

  1. extractionextracted with EtOAc
  2. dry with materialThe extracts were dried over Na2SO4
  3. filtrationfiltered
  4. concentrationconcentrated under reduced pressure
  5. customThe crude product was purified by column chromatography (SiO2, EtOAc:Hexane=20:80 to 80:10)

Quellen und Nachweise

ORD-Eintrag
ord-2b8a05fa91534d4ea23c603c5e333622
Quelldatensatz
uspto-grants-2012_07
Patentnummer
US08222248B2

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