Dimethylformamide → [3-(4-{2-butyl-1-[4-(2,4-dichloro-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amine

HRID 17705

Reaction equation

HRID 17705 reaction equation
[Cl:1][C:2]1[CH:15]=[C:14]([Cl:16])[CH:13]=[CH:12][C:3]=1[O:4][C:5]1[CH:11]=[CH:10][C:8]([NH2:9])=[CH:7][CH:6]=1.C[N:18]([CH:20]=O)C.Br[CH2:23][C:24]([C:26]1[CH:31]=[CH:30][C:29]([O:32][CH2:33][CH2:34][CH2:35][N:36]([CH2:39][CH3:40])[CH2:37][CH3:38])=[CH:28][CH:27]=1)=O>O.CCOC(C)=O>[CH2:15]([C:20]1[N:9]([C:8]2[CH:7]=[CH:6][C:5]([O:4][C:3]3[CH:12]=[CH:13][C:14]([Cl:16])=[CH:15][C:2]=3[Cl:1])=[CH:11][CH:10]=2)[CH:23]=[C:24]([C:26]2[CH:31]=[CH:30][C:29]([O:32][CH2:33][CH2:34][CH2:35][N:36]([CH2:39][CH3:40])[CH2:37][CH3:38])=[CH:28][CH:27]=2)[N:18]=1)[CH2:2][CH2:3][CH3:12]

Participants

6

Procedure

To a stirred solution of 4-(2,4-dichloro-phenoxy)aniline described above (1.2 eq., 5.2 mmol) in anhydrous DMF (20 mL) DIEA (3 eq. 15 mmol) was added, followed by slow addition of the 2-bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone described above (4.4 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 purified by chromatography (Silica gel). Pure product obtained from 2-4% MeOH/DCM (yield˜5%).

Workup

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

Sources & evidence

ORD record
ord-87a8c2665d60444d8cefb43d28d919e3
Source dataset
uspto-grants-2010_06
Patent number
US07737285B2

Linked notes

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