Water → Gamma-glutamyl-valyl-glycine

HRID 1946238Notes

Reaction equation

HRID 1946238 reaction equation
[NH:1](C(OCC1C=CC=CC=1)=O)[C@H:2]([C:26]([O:28]CC1C=CC=CC=1)=[O:27])[CH2:3][CH2:4][C:5]([NH:7][C@H:8]([C:12]([NH:14][CH2:15][C:16]([O:18]CC1C=CC=CC=1)=[O:17])=[O:13])[CH:9]([CH3:11])[CH3:10])=[O:6].O>C(O)C.[Pd]>[NH2:1][C@H:2]([C:26]([OH:28])=[O:27])[CH2:3][CH2:4][C:5]([NH:7][C@H:8]([C:12]([NH:14][CH2:15][C:16]([OH:18])=[O:17])=[O:13])[CH:9]([CH3:11])[CH3:10])=[O:6]

Participants

5

Procedure

Z-Glu(Val-Gly-OBzl)-OBzl described above (6.20 g, 10.03 mmol) was suspended in ethanol (200 ml), 10% palladium/carbon (1.50 g) was added to the suspension, and a reduction reaction was performed under a hydrogen atmosphere at 55° C. for 5 hours. During the reaction, 100 ml in a total volume of water was gradually added. The catalyst was removed by filtration using a Kiriyama funnel, and the filtrate was concentrated under reduced pressure to a half volume. The reaction solution was further filtered through a membrane filter, and the filtrate was concentrated under reduced pressure. After the residue was dissolved in a small volume of water, ethanol was added to precipitate a crystal, and the crystal was collected by filtration and dried under reduced pressure to obtain γ-Glu-Val-Gly as a white powder (2.85 g, 9.40 mmol).

Workup

  1. customa reduction reaction
  2. additionwas gradually added
  3. customThe catalyst was removed by filtration
  4. concentrationthe filtrate was concentrated under reduced pressure to a half volume
  5. filtrationThe reaction solution was further filtered through a membrane
  6. filtrationfilter
  7. concentrationthe filtrate was concentrated under reduced pressure
  8. dissolutionAfter the residue was dissolved in a small volume of water, ethanol
  9. additionwas added
  10. customto precipitate a crystal
  11. filtrationthe crystal was collected by filtration
  12. customdried under reduced pressure

Sources & evidence

ORD record
ord-a019f3a091a34672b9c4b1838a5ca6c9
Source dataset
uspto-grants-2013_03
Patent number
US08399417B2

Reaction notes

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