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

HRID 901695

Reaction equation

HRID 901695 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

Reactant 3

HCID 6228DimethylformamideHCID 269404-(2,4-Dichlorophenoxy)benzenamineHCID 865919692-Bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone

Product 1

HCID 59699284[3-(4-{2-butyl-1-[4-(2,4-dichloro-phenoxy)-phenyl]-1H-imidazol-4-yl}-phenoxy)-propyl]-diethyl-amine

Reagents, catalysts & solvents 2

HCID 962WaterSolventHCID 8857Ethyl AcetateSolvent

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-5dccb1a85b994bc1876d0bc079acf50c
Source dataset
uspto-grants-2008_04
Patent number
US07361678B2

Linked notes

Loading…