Trifluoroacetic acid → HCID 86595985, compound
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]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
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
- concentrationconcentrated under reduced pressure
- customThe residue was purified by silica gel flash column chromatography
- 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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