N-{[(2-{4-[6-chloro-2-(1-hydroxyethyl)-5-(trifluoromethyl)-1H-benzimidazol-1-yl]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide → N-{[(2-{4-[2-acetyl-6-chloro-5-(trifluoromethyl)-1H-benzimidazol-1-yl]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide

HRID 50459Notes

Reaction equation

HRID 50459 reaction equation
[Cl:1][C:2]1[C:3]([C:36]([F:39])([F:38])[F:37])=[CH:4][C:5]2[N:9]=[C:8]([CH:10]([OH:12])[CH3:11])[N:7]([C:13]3[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][NH:21][C:22]([NH:24][S:25]([C:28]4[CH:33]=[CH:32][C:31]([CH3:34])=[CH:30][CH:29]=4)(=[O:27])=[O:26])=[O:23])=[CH:15][CH:14]=3)[C:6]=2[CH:35]=1>C(Cl)Cl.O=[Mn]=O>[C:10]([C:8]1[N:7]([C:13]2[CH:18]=[CH:17][C:16]([CH2:19][CH2:20][NH:21][C:22]([NH:24][S:25]([C:28]3[CH:33]=[CH:32][C:31]([CH3:34])=[CH:30][CH:29]=3)(=[O:27])=[O:26])=[O:23])=[CH:15][CH:14]=2)[C:6]2[CH:35]=[C:2]([Cl:1])[C:3]([C:36]([F:38])([F:39])[F:37])=[CH:4][C:5]=2[N:9]=1)(=[O:12])[CH3:11]

Participants

4

Procedure

A solution of 1-[6-chloro-1-[4-(2-chloroethyl)phenyl]-5-(trifluoromethyl)-1H-benzimidazol-2-yl]ethanol (Example 367, step 1, 400 mg, 1 mmol) in CH2Cl2 was added MnO2 (2.7 g, 32 mmol) . The mixture was stirred at room temperature for 24 h. This was directly purified by flash column chromatography eluting with hexane/ethyl acetate (4:1) to afford 350 mg (88%) of the title compound as white solids.

Workup

  1. customThis was directly purified by flash column chromatography
  2. washeluting with hexane/ethyl acetate (4:1)

Sources & evidence

ORD record
ord-b5676d1a0703492db75a3f35f180e938
Source dataset
uspto-grants-2004_03
Patent number
US06710054B2

Reaction notes

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