Trifluoroacetic acid → HCID 68592521, compound
Reaction equation
C([O:5][C:6]([CH:8]1[CH2:12][CH:11]([O:13][C:14]2[CH:19]=[C:18]([C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][CH:21]=3)[N:17]=[C:16]([C:26]3[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=3)[N:15]=2)[CH2:10][CH:9]1[C:32](=[O:44])[NH:33][C:34]1([C:39]([O:41][CH2:42][CH3:43])=[O:40])[CH2:36][CH:35]1[CH:37]=[CH2:38])=[O:7])(C)(C)C.C([SiH](CC)CC)C.C(O)(C(F)(F)F)=O>>[C:26]1([C:16]2[N:15]=[C:14]([O:13][CH:11]3[CH2:12][CH:8]([C:6]([OH:7])=[O:5])[CH:9]([C:32](=[O:44])[NH:33][C:34]4([C:39]([O:41][CH2:42][CH3:43])=[O:40])[CH2:36][CH:35]4[CH:37]=[CH2:38])[CH2:10]3)[CH:19]=[C:18]([C:20]3[CH:21]=[CH:22][CH:23]=[CH:24][CH:25]=3)[N:17]=2)[CH:31]=[CH:30][CH:29]=[CH:28][CH:27]=1Participants
4
Procedure
Compound 17b (1.2 g, 2 mmol) was treated with triethylsilane (0.58 g, 5.0 mmol) and TFA (25 ml) according to the procedure described in Example 13 step b, which gave the crude title compound, (1.2 g), (M+H)+542.
Sources & evidence
- ORD record
- ord-759135089656412b9a849d615d42b322
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937080B2
Reaction notes
Loading…