HCID 15385777, compound → HCID 15385778, compound

HRID 1531665Notes

Reaction equation

HRID 1531665 reaction equation
[CH2:1]([S:3]([NH:6][C@@H:7]([C:15]([N:17]1[CH2:31][CH2:30][CH2:29][C@H:18]1[C:19]([O:21]CC1C=CC=CC=1)=[O:20])=[O:16])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:5])=[O:4])[CH3:2]>C(OCC)(=O)C.[Pd]>[CH2:1]([S:3]([NH:6][C@@H:7]([C:15]([N:17]1[CH2:31][CH2:30][CH2:29][C@H:18]1[C:19]([OH:21])=[O:20])=[O:16])[CH2:8][C:9]1[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=1)(=[O:5])=[O:4])[CH3:2]

Participants

4

Procedure

To a solution of EtSO2-D-Phe-Pro-OBn (28.5 g, 64 mmol) in ethyl acetate (500 mL) was added 10% Pd/C (5 g). The vessel was evacuated and placed under an atmosphere of hydrogen. After stirring for 16 h, the solution was filtered over diatomaceous earth, and the filter pad was then washed twice with methanol and filtered. The combined filtrates were concentrated in vacuo to give 22 g (97%) of off-white solid.

Workup

  1. customThe vessel was evacuated
  2. filtrationthe solution was filtered over diatomaceous earth
  3. washthe filter pad was then washed twice with methanol
  4. filtrationfiltered
  5. concentrationThe combined filtrates were concentrated in vacuo

Sources & evidence

ORD record
ord-c57de066d82b4c1b9bb85d0a05a0be2d
Source dataset
uspto-grants-2001_03
Patent number
US06200967B1

Reaction notes

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