HCID 59420727, compound → HCID 59420747, compound
Reaction equation
[F:1][C:2]([F:26])([F:25])[CH2:3][N:4]1[CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([S:13][Si](C(C)C)(C(C)C)C(C)C)[CH:10]=2)[C:5]1=[O:24]>Cl.CO.O1CCCC1>[F:26][C:2]([F:1])([F:25])[CH2:3][N:4]1[CH2:12][C:11]2[C:6](=[CH:7][CH:8]=[C:9]([SH:13])[CH:10]=2)[C:5]1=[O:24]Participants
5
Reactant 1
Product 1
Reagents, catalysts & solvents 3
Procedure
2-(2,2,2-trifluoroethyl)-5-((triisopropylsilyl)sulfanyl)isoindolin-1-one was dissolved in a solution of hydrochloric acid in methanol (2 ml) and tetrahydrofuran (2 ml) and stirred at room temperature for 2 hours or until disappearance of starting material. Reaction mixture concentrated to give desired material (quant yield). ES+ 248
Workup
- customReaction mixture
- concentrationconcentrated
Sources & evidence
- ORD record
- ord-e3cbe73007e74462ad4fc2217bcd68b0
- Source dataset
- uspto-grants-2010_08
- Patent number
- US07767672B2
Reaction notes
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