Triacetoxyperiodinane → HCID 58799012, compound
Reaction equation
[F:1][C:2]1[CH:3]=[C:4]([NH:21][C:22](=[O:34])[CH2:23][C:24]([NH:26][C:27]2[CH:32]=[CH:31][C:30]([F:33])=[CH:29][CH:28]=2)=[O:25])[CH:5]=[CH:6][C:7]=1[O:8][C:9]1[C:14]2=[C:15]([CH3:20])[C:16]([CH2:18][OH:19])=[CH:17][N:13]2[N:12]=[CH:11][N:10]=1.CC(OI1(OC(C)=O)(OC(C)=O)OC(=O)C2C=CC=CC1=2)=O>C1COCC1>[F:1][C:2]1[CH:3]=[C:4]([NH:21][C:22](=[O:34])[CH2:23][C:24]([NH:26][C:27]2[CH:28]=[CH:29][C:30]([F:33])=[CH:31][CH:32]=2)=[O:25])[CH:5]=[CH:6][C:7]=1[O:8][C:9]1[C:14]2=[C:15]([CH3:20])[C:16]([CH:18]=[O:19])=[CH:17][N:13]2[N:12]=[CH:11][N:10]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
To a solution of N1-(3-fluoro-4-(6-(hydroxymethyl)-5-methylpyrrolo[2,1-f][1,2,4]triazin-4-yloxy)phenyl)-N3-(4-fluorophenyl)malonamide (12 mg, 0.026 mmol, Example 41) in 1 mL of THF was added Dess-Martin periodinane (48 mg, 0.11 mmol, Aldrich) at room temperature. The mixture was allowed to stir for 2 h and HPLC analysis indicated total consumption of the starting material. The mixture was filtered through a plug of SiO2, washed with EtOAc. The organic solvent was then removed under reduced pressure and the residue was purified on preparative HPLC to afford the title compound (10 mg, 83%). MS(ESI+) m/z 466.2 (M+H)+.
Workup
- customconsumption of the starting material
- filtrationThe mixture was filtered through a plug of SiO2
- washwashed with EtOAc
- customThe organic solvent was then removed under reduced pressure
- customthe residue was purified on preparative HPLC
Sources & evidence
- ORD record
- ord-fe279e4a16f145d0a80fd0933d557c60
- Source dataset
- uspto-grants-2007_02
- Patent number
- US07173031B2
Reaction notes
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