Chlorotrimethylsilane → HCID 86599797, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([S:8][C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[C:15]([C:18]([OH:20])=[O:19])[CH:16]=3)[NH:11][C:10]=2[CH3:21])=[CH:4][CH:3]=1.[CH3:22][Si](Cl)(C)C>CO>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]([S:8][C:9]2[C:17]3[C:12](=[CH:13][CH:14]=[C:15]([C:18]([O:20][CH3:22])=[O:19])[CH:16]=3)[NH:11][C:10]=2[CH3:21])=[CH:6][CH:7]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution/suspension of the product from part (i) (1 g) in methanol (50 ml) was added trimethylsilylchloride (12.6 ml). After stirring at room temperture overnight the mixture was concentrated in vacuo to give sub-title compound in quantitative yield.
Workup
- concentrationwas concentrated in vacuo
Sources & evidence
- ORD record
- ord-0acaa362b6954244bc24e92122dd0384
- Source dataset
- uspto-grants-2007_01
- Patent number
- US07166607B2
Reaction notes
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