Water → HCID 15230547, compound

HRID 1613311Notes

Reaction equation

HRID 1613311 reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1/[C:8](/[C:34]1[CH:39]=[CH:38][C:37]([O:40][CH3:41])=[CH:36][CH:35]=1)=[CH:9]\[C:10]([N:12]1[CH2:17][CH2:16][N:15]([C:18](=[O:33])[C:19]2[CH:24]=[C:23]([O:25][CH3:26])[C:22]([O:27]C(=O)C)=[C:21]([O:31][CH3:32])[CH:20]=2)[CH2:14][CH2:13]1)=[O:11].C(=O)([O-])[O-].[K+].[K+].O>CO>[Cl:1][C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][C:3]=1/[C:8](/[C:34]1[CH:35]=[CH:36][C:37]([O:40][CH3:41])=[CH:38][CH:39]=1)=[CH:9]\[C:10]([N:12]1[CH2:17][CH2:16][N:15]([C:18](=[O:33])[C:19]2[CH:24]=[C:23]([O:25][CH3:26])[C:22]([OH:27])=[C:21]([O:31][CH3:32])[CH:20]=2)[CH2:14][CH2:13]1)=[O:11]

Participants

5

Procedure

To a solution of a compound of Example 91 (0.500 g) in methanol (20 ml) was added an aqueous solution saturated with potassium carbonate (10 ml), and the resulting mixture was stirred at room temperature for an hour. The reaction mixture was poured into water and extracted thrice with methylenechloride. The combined extract was washed with water, dried and concentrated. The residue was purified by liquid chromatography under medium pressure through two Lobar B columns. Fractions eluted with a 19:1 mixture of ethyl acetate and methanol were collected and worked up to afford the title compound (0.464 g) as a powder.

Workup

  1. extractionextracted thrice with methylenechloride
  2. extractionThe combined extract
  3. washwas washed with water
  4. customdried
  5. concentrationconcentrated
  6. customThe residue was purified by liquid chromatography under medium pressure through two Lobar B columns
  7. washFractions eluted with a 19:1 mixture of ethyl acetate and methanol
  8. customwere collected

Sources & evidence

ORD record
ord-f86cf37d82654bbca6e044c2c0651fce
Source dataset
uspto-grants-1993_03
Patent number
US05192766

Reaction notes

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