Citric Acid → HCID 57302818, compound

HRID 726435Notes

Reaction equation

HRID 726435 reaction equation
C([O:3][C:4](=[O:43])[C@@H:5]([NH:33][S:34]([C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)(=[O:36])=[O:35])[CH2:6][NH:7][C:8](=[O:32])[CH2:9][CH2:10][NH:11][C:12](=[O:31])[CH2:13][O:14][CH:15]1[CH2:20][CH2:19][N:18]([C:21]([O:23][CH2:24][C:25]2[CH:30]=[CH:29][CH:28]=[CH:27][CH:26]=2)=[O:22])[CH2:17][CH2:16]1)C.[OH-].[Na+].C(O)(=O)CC(CC(O)=O)(C(O)=O)O>CN(C=O)C>[C:37]1([S:34]([NH:33][C@@H:5]([CH2:6][NH:7][C:8](=[O:32])[CH2:9][CH2:10][NH:11][C:12](=[O:31])[CH2:13][O:14][CH:15]2[CH2:20][CH2:19][N:18]([C:21]([O:23][CH2:24][C:25]3[CH:26]=[CH:27][CH:28]=[CH:29][CH:30]=3)=[O:22])[CH2:17][CH2:16]2)[C:4]([OH:43])=[O:3])(=[O:36])=[O:35])[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1

Participants

5

Procedure

The compound (144 mg) obtained in the above (2) is dissolved in DMF (3 ml), and thereto is added 1N aqueous sodium hydroxide solution (698 μl) under ice-cooling, and the mixture is stirred for 1.5 hour. The pH value thereof is adjusted to pH 2 with 10% aqueous citric acid solution, and extracted three times with ethyl acetate. The extract is washed twice with a saturated brine, and dried over anhydrous magnesium sulfate. The desiccant is removed by filtration, and the filtrate is concentrated under reduced pressure to give the title compound (92 mg).

Workup

  1. temperaturecooling
  2. extractionextracted three times with ethyl acetate
  3. washThe extract is washed twice with a saturated brine
  4. dry with materialdried over anhydrous magnesium sulfate
  5. customThe desiccant is removed by filtration
  6. concentrationthe filtrate is concentrated under reduced pressure

Sources & evidence

ORD record
ord-af399f1256814ab081caad96d435d6f4
Source dataset
uspto-grants-1998_01
Patent number
US05707994

Reaction notes

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