Potassium Carbonate → methyl 3-chloro-4-((5-(2-(3,4-dichlorophenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-yl)methoxy)-5-fluorobenzoate

HRID 83922ノート

反応式

HRID 83922 の反応式
Cl[CH2:2][C:3]1[N:4]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=2)[C:5]([C:8]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([Cl:18])[CH:12]=2)([CH3:10])[CH3:9])=[CH:6][N:7]=1.[Cl:26][C:27]1[CH:28]=[C:29]([CH:34]=[C:35]([F:38])[C:36]=1[OH:37])[C:30]([O:32][CH3:33])=[O:31].C(=O)([O-])[O-].[K+].[K+].C1OCCOCCOCCOCCOCCOC1>CC#N>[Cl:26][C:27]1[CH:28]=[C:29]([CH:34]=[C:35]([F:38])[C:36]=1[O:37][CH2:2][C:3]1[N:4]([C:19]2[CH:24]=[CH:23][C:22]([F:25])=[CH:21][CH:20]=2)[C:5]([C:8]([C:11]2[CH:16]=[CH:15][C:14]([Cl:17])=[C:13]([Cl:18])[CH:12]=2)([CH3:9])[CH3:10])=[CH:6][N:7]=1)[C:30]([O:32][CH3:33])=[O:31]

参加物

6

反応物 4

HCID 11430Potassium CarbonateHCID 2855718-Crown-6HCID 66619271Methyl 3-chloro-5-fluoro-4-hydroxybenzoateHCID 667400042-(chloromethyl)-5-(2-(3,4-dichlorophenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazole

生成物 1

HCID 66740309methyl 3-chloro-4-((5-(2-(3,4-dichlorophenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-yl)methoxy)-5-fluorobenzoate収率 68%

試薬・触媒・溶媒 1

HCID 6342Acetonitrile溶媒

反応条件

温度
60 °C

実験手順

A mixture of 2-(chloromethyl)-5-(2-(3,4-dichlorophenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazole (154 mg, 0.39 mmol), methyl 3-chloro-5-fluoro-4-hydroxybenzoate (118 mg 0.57 mmol), potassium carbonate (79 mg, 0.57 mmol), and 18-crown-6 (11 mg, 0.04 mmol) in CH3CN (4 mL) was heated 8 h at 60° C. After cooling, the reaction mixture was filtered, combined with water and DCM, and then extracted further with DCM. The combined extracts were washed with brine, dried over Na2SO4, and concentrated in vacuo. The material was purified by chromatography (silica, 0-70% EtOAc/Hex) to give methyl 3-chloro-4-((5-(2-(3,4-dichlorophenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazol-2-yl)methoxy)-5-fluorobenzoate as a white solid (150 mg, 68% yield). MS (EI) m/z 567.3 [M+H]+.

後処理

  1. temperatureAfter cooling
  2. filtrationthe reaction mixture was filtered
  3. extractionextracted further with DCM
  4. washThe combined extracts were washed with brine
  5. dry with materialdried over Na2SO4
  6. concentrationconcentrated in vacuo
  7. customThe material was purified by chromatography (silica, 0-70% EtOAc/Hex)

出典と根拠

ORDレコード
ord-9e77f86e596142c1b1e3e0074338f36a
出典データセット
uspto-grants-2014_09
特許番号
US08846739B2

反応ノート

読み込み中…