Water → HCID 178492501, compound

HRID 63237Notes

Reaction equation

HRID 63237 reaction equation
C1(S([N:10]2[CH:14]=[C:13]([C:15]([C:17]3[CH:22]=[C:21]([O:23][CH3:24])[C:20]([O:25][CH3:26])=[C:19]([O:27][CH3:28])[CH:18]=3)=[O:16])[N:12]=[C:11]2[C:29]2[CH:30]=[C:31]3[C:35](=[CH:36][CH:37]=2)[N:34](S(C2C=CC=CC=2)(=O)=O)[C:33]([C:47](=[O:60])[C:48]2[CH:53]=[C:52]([O:54][CH3:55])[C:51]([O:56][CH3:57])=[C:50]([O:58][CH3:59])[CH:49]=2)=[CH:32]3)(=O)=O)C=CC=CC=1.[OH-].[Na+].O>C(O)C>[CH3:24][O:23][C:21]1[CH:22]=[C:17]([CH:18]=[C:19]([O:27][CH3:28])[C:20]=1[O:25][CH3:26])[C:15]([C:13]1[N:12]=[C:11]([C:29]2[CH:30]=[C:31]3[C:35](=[CH:36][CH:37]=2)[NH:34][C:33]([C:47]([C:48]2[CH:49]=[C:50]([O:58][CH3:59])[C:51]([O:56][CH3:57])=[C:52]([O:54][CH3:55])[CH:53]=2)=[O:60])=[CH:32]3)[NH:10][CH:14]=1)=[O:16]

Participants

5

Procedure

To a solution of (1-(phenylsulfonyl)-2-(1-(phenylsulfonyl)-2-(3,4,5-trimethoxybenzoyl)-1H-indol-5-yl)-1H-imidazol-4-yl)(3,4,5-trimethoxyphenyl)methanone (16xaa) (1 mmol) in ethanol (20 mL) was added sodium hydroxide (10 equiv) and stirred overnight in darkness. The reaction mixture was diluted by 50 mL of water and extracted by ethyl acetate (250 mL). The organic layer was dried over magnesium sulfate and concentrated. The residue was purified by flash column chromatography (hexane:ethyl acetate 3:1) or recrystallized from water and methanol to give a white solid. Yield: 30-95%.

Workup

  1. extractionextracted by ethyl acetate (250 mL)
  2. dry with materialThe organic layer was dried over magnesium sulfate
  3. concentrationconcentrated
  4. customThe residue was purified by flash column chromatography (hexane:ethyl acetate 3:1)
  5. customrecrystallized from water and methanol
  6. customto give a white solid

Sources & evidence

ORD record
ord-2ad887c684004faeb4b2a22c4074138e
Source dataset
uspto-grants-2016_09
Patent number
US09447049B2

Reaction notes

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