Trimethylsilyl iodide → HCID 67501441, compound
Reaction equation
[Na:1].N1(C(C[C@H](CO)OCP(O)(O)=O)=O)C=C(C)C(=O)NC1=O.[N:23]1([C:31]([CH2:33][C@H:34]([CH2:47][OH:48])[O:35][CH2:36][P:37]([O:43]C(C)C)([O:39]C(C)C)=[O:38])=[O:32])[CH:30]=[CH:29][C:27]([NH2:28])=[N:26][C:24]1=[O:25].I[Si](C)(C)C>>[Na:1].[N:23]1([C:31]([CH2:33][C@H:34]([CH2:47][OH:48])[O:35][CH2:36][P:37]([OH:39])([OH:43])=[O:38])=[O:32])[CH:30]=[CH:29][C:27]([NH2:28])=[N:26][C:24]1=[O:25]Participants
4
Procedure
This compound was prepared as described for 3f, using 22 (200 mg, 0.53 mmol) as a starting material and iodotrimethysilane (0.6 mL, 4.2 mmol). Compound 3h (130 mg, 0.38 mmol) was obtained as a colorless solid, in 73% yield, which was characterized as follows:
Workup
- customThis compound was prepared
Sources & evidence
- ORD record
- ord-5220f0fab1b64a7a975f07df73e9d499
- Source dataset
- uspto-grants-2016_02
- Patent number
- US09249177B2
Reaction notes
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