Hydrochloric Acid → SB 203580, Sulfone

HRID 2293493Notes

Reaction equation

HRID 2293493 reaction equation
[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([C:19]3[CH:24]=[CH:23][C:22]([S:25]([CH3:27])=[O:26])=[CH:21][CH:20]=3)[NH:11][C:12]=2[C:13]2[CH:18]=[CH:17][N:16]=[CH:15][CH:14]=2)=[CH:4][CH:3]=1.Cl.O.[O-:30][Mn](=O)(=O)=O.[K+].[O-]S([O-])=O.[Na+].[Na+].Cl.[OH-].[Na+]>O>[F:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[N:9]=[C:10]([C:19]3[CH:24]=[CH:23][C:22]([S:25]([CH3:27])(=[O:30])=[O:26])=[CH:21][CH:20]=3)[NH:11][C:12]=2[C:13]2[CH:14]=[CH:15][N:16]=[CH:17][CH:18]=2)=[CH:4][CH:3]=1

Participants

8

Procedure

To a solution of 4-(4-fluorophenyl)-2-(4-methylsulfinylphenyl)-5-(4-pyridyl)-1H-imidazole (3.7 g, 9.8 mmol) [See Ex. 20 below] in 1:10 3N HCl/H2O (88 mL) was added a solution of KMnO4 (1.5 g, 9.8 mmol) in H2O (15 mL). After sting at rt for 1 h, additional KMnO4 (0.15 g, 0.9 mmol) was added, and sting was continued for 15 min. The mixture was then poured into saturated aqueous Na2SO3 (200 mL), and the pH was adjusted to slightly acidic by the addition of 3N HCl, then to neutral by the addition of 2.5N NaOH. The solid which formed was collected by filtration, washed successively with H2O and MeOH and recrystallized three times from MeOH to afford the title compound (0.63 g, 16%): mp 148°-149° C.

Workup

  1. waitsting was continued for 15 min
  2. customThe solid which formed
  3. filtrationwas collected by filtration
  4. washwashed successively with H2O and MeOH
  5. customrecrystallized three times from MeOH

Sources & evidence

ORD record
ord-14c16e2db56f4046a8244c85b2834ddf
Source dataset
uspto-grants-1997_11
Patent number
US05686455

Reaction notes

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