Potassium Carbonate → 2-(4-bromo-2,6-difluorobenzylthio)-5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazole

HRID 83839Notes

Reaction equation

HRID 83839 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]([C:11]2[N:15]([C:16]3[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=3)[C:14]([SH:23])=[N:13][CH:12]=2)([CH3:10])[CH3:9])=[CH:4][C:3]=1[O:24][CH3:25].[Br:26][C:27]1[CH:28]=[C:29]([F:36])[C:30]([CH2:34]Br)=[C:31]([F:33])[CH:32]=1.C(=O)([O-])[O-].[K+].[K+]>CC(C)=O>[Br:26][C:27]1[CH:28]=[C:29]([F:36])[C:30]([CH2:34][S:23][C:14]2[N:15]([C:16]3[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=3)[C:11]([C:8]([C:5]3[CH:6]=[CH:7][C:2]([Cl:1])=[C:3]([O:24][CH3:25])[CH:4]=3)([CH3:10])[CH3:9])=[CH:12][N:13]=2)=[C:31]([F:33])[CH:32]=1

Participants

5

Procedure

A mixture of 5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazole-2-thiol (1.5 g, 4.0 mmol, 1.0 eq), 5-bromo-2-(bromomethyl)-1,3-difluorobenzene (1.37 g, 4.8 mmol, 1.2 eq) and potassium carbonate (830 mg, 6.0 mmol, 1.5 eq) in acetone (20 mL) was stirred at room temperature overnight. The mixture was filtered and the filtrate was concentrated and purified by chromatography (silica, 0 to 60% EtOAc/Hex) to provide 2-(4-bromo-2,6-difluorobenzylthio)-5-(2-(4-chloro-3-methoxyphenyl)propan-2-yl)-1-(4-fluorophenyl)-1H-imidazole (1.96 g (85%) as a beige solid: 1H NMR (400 MHz, CDCl3) δ 7.56 (s, 1H), 7.27-7.20 (m, 1H), 7.10-7.00 (m, 2H), 6.93-6.82 (m, 2H), 6.51-6.44 (m, 2H), 6.42-6.32 (m, 2H), 4.59 (s, 2H), 3.81-3.76 (m, 3H), 1.55 (d, J=10.3 Hz, 6H).

Workup

  1. filtrationThe mixture was filtered
  2. concentrationthe filtrate was concentrated
  3. custompurified by chromatography (silica, 0 to 60% EtOAc/Hex)

Sources & evidence

ORD record
ord-808a70cb23be462ab5f75d7d2bc45180
Source dataset
uspto-grants-2014_09
Patent number
US08846739B2

Reaction notes

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