Trifluoroacetic acid → HCID 59463765, compound
Reaction equation
C(O)(C(F)(F)F)=O.C(OC(=O)[NH:14][CH2:15][CH:16]([CH2:27][O:28][C:29]([C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)([C:36]1[CH:41]=[CH:40][CH:39]=[CH:38][CH:37]=1)[C:30]1[CH:35]=[CH:34][CH:33]=[CH:32][CH:31]=1)[CH2:17][CH2:18][N:19]1[CH:24]=[CH:23][C:22](=[O:25])[NH:21][C:20]1=[O:26])(C)(C)C>ClCCl>[NH2:14][CH2:15][CH:16]([CH2:27][O:28][C:29]([C:42]1[CH:43]=[CH:44][CH:45]=[CH:46][CH:47]=1)([C:36]1[CH:37]=[CH:38][CH:39]=[CH:40][CH:41]=1)[C:30]1[CH:31]=[CH:32][CH:33]=[CH:34][CH:35]=1)[CH2:17][CH2:18][N:19]1[CH:24]=[CH:23][C:22](=[O:25])[NH:21][C:20]1=[O:26]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
TFA (2 ml) was added to a solution of compound 42 (100 mg, 0.18 mmol) in dichloromethane (4 ml) and the solution was stirred at room temperature. After 30 min the solvents were evaporated in vacuo and the afforded residue was purified by column chromatography on silica gel which gave the title compound (52 mg, 65%).
Workup
- customAfter 30 min the solvents were evaporated in vacuo
- customthe afforded residue was purified by column chromatography on silica gel which
Sources & evidence
- ORD record
- ord-6614962b560742cbb904a1d95279d8ee
- Source dataset
- uspto-grants-2011_09
- Patent number
- US08017620B2
Reaction notes
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