HCID 12112580, compound → HCID 12112584, compound
Reaction equation
[OH:1]OS([O-])=O.[K+].[CH3:7][C:8]1[O:12][C:11]([C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][CH:21]=2)[O:18][CH2:17][O:16]3)=[N:10][C:9]=1[CH2:22][C:23]1[O:27][C:26](/[CH:28]=[CH:29]/[CH2:30][S:31][CH2:32][C:33]([OH:35])=[O:34])=[CH:25][CH:24]=1>O1CCCC1>[CH3:7][C:8]1[O:12][C:11]([C:13]2[CH:14]=[C:15]3[C:19](=[CH:20][CH:21]=2)[O:18][CH2:17][O:16]3)=[N:10][C:9]=1[CH2:22][C:23]1[O:27][C:26](/[CH:28]=[CH:29]/[CH2:30][S:31]([CH2:32][C:33]([OH:35])=[O:34])=[O:1])=[CH:25][CH:24]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
A aqueous solution (100 ml) of OXONE (trade mark) (891 mg) was added dropwise to a solution of the compound prepared in Example 3(2) (1.0 g) in tetrahydrofuran (200 ml) over a period of 30 minutes at −2˜−3° C., and the resultant solution was stirred for 10 minutes at 0° C. Ice water was added to the reaction solution, and the resultant solution was extracted with ethyl acetate, and the extract was washed with water and a saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate, and concentrated. The residue was purified by silica gel column chromatography (chloroform:methanol=50:1→10:1) to give the title compound (750 mg) having the following physical data.
Workup
- extractionthe resultant solution was extracted with ethyl acetate
- washthe extract was washed with water
- dry with materiala saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate
- concentrationconcentrated
- customThe residue was purified by silica gel column chromatography (chloroform:methanol=50:1→10:1)
Sources & evidence
- ORD record
- ord-bb6cb6c0df28464e8a8f0b968b4ae3b8
- Source dataset
- uspto-grants-2004_11
- Patent number
- US06821994B2
Reaction notes
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