Trifluoroacetic acid → HCID 86595985, compound

HRID 2099704Notes

Reaction equation

HRID 2099704 reaction equation
C(O[C:6](=O)[N:7]([CH:9]([CH3:32])[CH2:10][C:11]1[CH:31]=[CH:30][C:14]2[O:15][CH:16]([CH2:18][NH:19][C:20]([O:22][CH2:23][C:24]3[CH:29]=[CH:28][CH:27]=[CH:26][CH:25]=3)=[O:21])[O:17][C:13]=2[CH:12]=1)C)(C)(C)C.[F:34][C:35]([F:40])([F:39])[C:36]([OH:38])=[O:37]>ClCCl>[F:34][C:35]([F:40])([F:39])[C:36]([OH:38])=[O:37].[CH2:23]([O:22][C:20](=[O:21])[NH:19][CH2:18][CH:16]1[O:15][C:14]2[CH:30]=[CH:31][C:11]([CH2:10][CH:9]([NH:7][CH3:6])[CH3:32])=[CH:12][C:13]=2[O:17]1)[C:24]1[CH:25]=[CH:26][CH:27]=[CH:28][CH:29]=1

Participants

4

Procedure

To a solution of 0.41 g (0.89 mmol) of 1G in 2 mL of dichloromethane was added 2 mL of trifluoroacetic acid. The resulting solution was allowed to stir at room temperature for 90 minutes and concentrated under reduced pressure. The residue was purified by silica gel flash column chromatography using 20% methanol in ethyl acetate to give 0.29 g (0.64 mmol, 69%) of 1H as a colorless thick gum (M+Na, 357).

Workup

  1. concentrationconcentrated under reduced pressure
  2. customThe residue was purified by silica gel flash column chromatography
  3. customto give 0.29 g (0.64 mmol, 69%) of 1H as a colorless thick gum (M+Na, 357)

Sources & evidence

ORD record
ord-2367317726dc4c389867db6a281891dd
Source dataset
uspto-grants-2009_08
Patent number
US07569676B2

Reaction notes

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