HCID 12112580, compound → HCID 12112584, compound

HRID 2416016Notes

Reaction equation

HRID 2416016 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]=1

Participants

4

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

  1. extractionthe resultant solution was extracted with ethyl acetate
  2. washthe extract was washed with water
  3. dry with materiala saturated aqueous solution of sodium chloride, dried over anhydrous magnesium sulfate
  4. concentrationconcentrated
  5. 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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