Trifluoroacetic acid → HCID 68592566, compound
Reaction equation
C([O:5][C:6]([CH:8]1[CH2:12][CH:11]([O:13][C:14]2[CH:19]=[C:18]([O:20][CH3:21])[N:17]=[C:16]([C:22]3[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=3)[N:15]=2)[CH2:10][CH:9]1[C:28](=[O:40])[NH:29][C:30]1([C:35]([O:37][CH2:38][CH3:39])=[O:36])[CH2:32][CH:31]1[CH:33]=[CH2:34])=[O:7])(C)(C)C.C([SiH](CC)CC)C.C(O)(C(F)(F)F)=O>C(Cl)Cl>[CH2:38]([O:37][C:35]([C:30]1([NH:29][C:28]([CH:9]2[CH2:10][CH:11]([O:13][C:14]3[CH:19]=[C:18]([O:20][CH3:21])[N:17]=[C:16]([C:22]4[CH:23]=[CH:24][CH:25]=[CH:26][CH:27]=4)[N:15]=3)[CH2:12][CH:8]2[C:6]([OH:7])=[O:5])=[O:40])[CH2:32][CH:31]1[CH:33]=[CH2:34])=[O:36])[CH3:39]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 7a (1.48 g, 2.68 mmol) was dissolved in 35 ml DCM. Triethylsilane (1.07 ml, 6.7 mmol) and 35 ml TFA were added and the mixture was stirred at RT for 45 minutes. The solvent was evaporated and co evaporated with toluene which gave the title product (1.32 g, 99%), MS (M+H)+496.
Workup
- customThe solvent was evaporated
- customco evaporated with toluene which
Sources & evidence
- ORD record
- ord-d9200c526a2f4821a33935f4f2627ddd
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937080B2
Reaction notes
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