Triethylsilane → HCID 68590308, 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][C:23]([O:26][CH3:27])=[CH:22][CH:21]=3)[N:17]=[C:16]([O:28][CH3:29])[N:15]=2)[CH2:10][CH:9]1[C:30](=[O:42])[NH:31][C:32]1([C:37]([O:39][CH2:40][CH3:41])=[O:38])[CH2:34][CH:33]1[CH:35]=[CH2:36])=[O:7])(C)(C)C.C([SiH](CC)CC)C>C(O)(C(F)(F)F)=O>[CH2:40]([O:39][C:37]([C:32]1([NH:31][C:30]([CH:9]2[CH2:10][CH:11]([O:13][C:14]3[CH:19]=[C:18]([C:20]4[CH:21]=[CH:22][C:23]([O:26][CH3:27])=[CH:24][CH:25]=4)[N:17]=[C:16]([O:28][CH3:29])[N:15]=3)[CH2:12][CH:8]2[C:6]([OH:7])=[O:5])=[O:42])[CH2:34][CH:33]1[CH:35]=[CH2:36])=[O:38])[CH3:41]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
Compound 16b (1.11 g, 1.9 mmol) was treated with triethylsilane (0.55 g, 4.75 mmol) and TFA (30 ml) according to the procedure described in Example 13 step b which gave the crude title compound, (1.3 g), (M+H)+526.
Sources & evidence
- ORD record
- ord-b79ff7b0ab444534adae7db7c196cf24
- Source dataset
- uspto-grants-2015_01
- Patent number
- US08937080B2
Reaction notes
Loading…