Water → HCID 21876478, compound

HRID 2077815Notes

Reaction equation

HRID 2077815 reaction equation
[NH2:1][CH:2]([C:4]1[N:8]([C:9]2[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][NH:17][C:18]([NH:20][S:21]([C:24]3[CH:29]=[CH:28][C:27]([CH3:30])=[CH:26][CH:25]=3)(=[O:23])=[O:22])=[O:19])=[CH:11][CH:10]=2)[C:7]2[CH:31]=[C:32]([Cl:39])[C:33]([C:35]([F:38])([F:37])[F:36])=[CH:34][C:6]=2[N:5]=1)[CH3:3].[C:40](Cl)(=[O:42])[CH3:41].O>C(Cl)Cl>[Cl:39][C:32]1[C:33]([C:35]([F:36])([F:38])[F:37])=[CH:34][C:6]2[N:5]=[C:4]([CH:2]([NH:1][C:40](=[O:42])[CH3:41])[CH3:3])[N:8]([C:9]3[CH:14]=[CH:13][C:12]([CH2:15][CH2:16][NH:17][C:18]([NH:20][S:21]([C:24]4[CH:29]=[CH:28][C:27]([CH3:30])=[CH:26][CH:25]=4)(=[O:23])=[O:22])=[O:19])=[CH:11][CH:10]=3)[C:7]=2[CH:31]=1

Participants

5

Procedure

A mixture of N-{[(2-{4-[2-(1-aminoethyl)-6-chloro-5-(trifluoromethyl)-1H-benzimidazol-1-yl]phenyl}ethyl)amino]carbonyl}-4-methylbenzenesulfonamide (step 3, 100 mg, 0.17 mmol) in CH2Cl2 (12 ml) was added acetyl chloride (0.01 ml, 0.18 mmol) and stirred at room temperature for 5 h. The mixture was added water (10 ml) and extracted with CH2Cl2 (20 ml). The organic layer was washed with brine (10 ml), then dried (Na2SO4). After removal of solvent, the crude product was purified by flash column chromatography eluting with CH2Cl2/MeOH (10:1) to afford 59 mg (53%) of the title compound as white solids.

Workup

  1. extractionextracted with CH2Cl2 (20 ml)
  2. washThe organic layer was washed with brine (10 ml)
  3. dry with materialdried (Na2SO4)
  4. customAfter removal of solvent
  5. customthe crude product was purified by flash column chromatography
  6. washeluting with CH2Cl2/MeOH (10:1)

Sources & evidence

ORD record
ord-847ddd8f93964b89b34ceeca680ab24e
Source dataset
uspto-grants-2011_04
Patent number
US07928119B2

Reaction notes

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