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

HRID 2237059Notes

Reaction equation

HRID 2237059 reaction equation
[Cl:1][C:2]1[CH:17]=[CH:16][C:5]([O:6][C:7]2[CH:12]=[CH:11][C:10]([N+:13]([O-])=O)=[CH:9][CH:8]=2)=[CH:4][C:3]=1[CH2:18][CH3:19].C[N:21]([CH:23]=O)C.Br[CH2:26][C:27]([C:29]1[CH:34]=[CH:33][C:32]([O:35][CH2:36][CH2:37][CH2:38][N:39]([CH2:42][CH3:43])[CH2:40][CH3:41])=[CH:31][CH:30]=1)=O>O.CCOC(C)=O>[CH2:17]([C:23]1[N:13]([C:10]2[CH:11]=[CH:12][C:7]([O:6][C:5]3[CH:16]=[CH:17][C:2]([Cl:1])=[C:3]([CH2:18][CH3:19])[CH:4]=3)=[CH:8][CH:9]=2)[CH:26]=[C:27]([C:29]2[CH:34]=[CH:33][C:32]([O:35][CH2:36][CH2:37][CH2:38][N:39]([CH2:42][CH3:43])[CH2:40][CH3:41])=[CH:31][CH:30]=2)[N:21]=1)[CH2:2][CH2:3][CH3:4]

Participants

6

Reactant 3

HCID 6228DimethylformamideHCID 669775234-(4-Chloro-3-ethylphenoxy)-1-nitrobenzeneHCID 865919692-Bromo-1-{4-[3-(diethylamino)propoxy]phenyl}ethanone

Product 1

HCID 59699350[3-(4-{2-butyl-1-[4-(4-chloro-3-ethyl-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-(4-chloro-3-ethylphenoxy)-1-nitrobenzene (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 (2.4 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 used for further transformation .

Workup

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

Sources & evidence

ORD record
ord-d14dac75f6c840f2b6de23a39ce7877b
Source dataset
uspto-grants-2010_05
Patent number
US07714013B2

Reaction notes

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