Dimethylformamide → 2-butyl-4-[4-(4-ethyl-hexyloxy)-phenyl]-1-[4-(4-methoxy-naphthalen-1-yl-oxy)-phenyl]-1H-imidazole

HRID 17718Notizen

Reaktionsgleichung

Reaktionsgleichung von HRID 17718
[CH3:1][O:2][C:3]1[C:12]2[C:7](=[CH:8][CH:9]=[CH:10][CH:11]=2)[C:6]([O:13][C:14]2[CH:20]=[CH:19][C:17]([NH2:18])=[CH:16][CH:15]=2)=[CH:5][CH:4]=1.C[N:22]([CH:24]=O)C.Br[CH2:27][C:28]([C:30]1[CH:35]=[CH:34][C:33]([O:36][CH2:37][CH2:38][CH2:39]N(CC)CC)=[CH:32][CH:31]=1)=O>O.CCOC(C)=O>[CH2:6]([C:24]1[N:18]([C:17]2[CH:16]=[CH:15][C:14]([O:13][C:6]3[C:7]4[C:12](=[CH:11][CH:10]=[CH:9][CH:8]=4)[C:3]([O:2][CH3:1])=[CH:4][CH:5]=3)=[CH:20][CH:19]=2)[CH:27]=[C:28]([C:30]2[CH:31]=[CH:32][C:33]([O:36][CH2:37][CH2:38][CH2:39][CH:3]([CH2:12][CH3:11])[CH2:4][CH3:5])=[CH:34][CH:35]=2)[N:22]=1)[CH2:7][CH2:8][CH3:9]

Komponenten

6

Versuchsvorschrift

To a stirred solution of 4-(4-methoxy-naphthalen-1-yloxy)aniline (1.2 eq., 2.5 mmol) in anhydrous DMF (5 mL) DIEA (3 eq. 7.5 mmol) was added, followed by slow addition of the 2-bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone described above (2.3 mmol), according to General Procedure R2. The reaction mixture was stirred under nitrogen at rt until completion, as indicated by TLC or HPLC. The reaction mixture was then diluted with cold H2O and the product was isolated in EtOAc. The combined organic layers were washed with brine and dried over sodium sulfate. Evaporation of solvent in vacuuo afforded the desired product. The crude alkylated aniline was used for further transformation.

Aufarbeitung

  1. washThe combined organic layers were washed with brine
  2. dry with materialdried over sodium sulfate
  3. customEvaporation of solvent in vacuuo

Quellen und Nachweise

ORD-Eintrag
ord-fb4eae6a0373474f830e11cc54fd4c87
Quelldatensatz
uspto-grants-2010_06
Patentnummer
US07737285B2

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