Hydrochloric Acid → HCID 131720451, compound
Reaction equation
[NH:1]([C:30]([O:32][CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)=[O:31])[C@H:2]([C:7]([NH:9][C@H:10]([C:15]([NH:17][CH:18]([C:23](C(OCC)=O)=[O:24])[CH2:19][CH2:20][CH2:21][CH3:22])=[O:16])[CH2:11][CH:12]([CH3:14])[CH3:13])=[O:8])[CH2:3][CH:4]([CH3:6])[CH3:5].[OH-:40].[Na+].Cl>CO>[NH:1]([C:30]([O:32][CH2:33][C:34]1[CH:39]=[CH:38][CH:37]=[CH:36][CH:35]=1)=[O:31])[C@H:2]([C:7]([NH:9][C@H:10]([C:15]([NH:17][CH:18]([C:23]([OH:24])=[O:40])[CH2:19][CH2:20][CH2:21][CH3:22])=[O:16])[CH2:11][CH:12]([CH3:13])[CH3:14])=[O:8])[CH2:3][CH:4]([CH3:6])[CH3:5]Participants
5
Reactant 3
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 0 °C
Procedure
To a stirred solution of N-Cbz-L-Leu-L-Leu-DL-Nle-CO2Et (1.0 eq), as prepared in Example 5, in methanol at R.T. is added 1N NaOH (1.1 eq). The mixture is stirred for 6 h. The reaction mixture is cooled to 0° C., acidified with 1N HCl (pH=3) and extracted with EA. The organic extracts are washed with water, dried (MgSO4), filtered and concentrated to give a crude residue. Trituration with hexane and drying in vacuo gives the title compound, N-Cbz-L-Leu-L-Leu-DL-Nle-CO2H.
Workup
- extractionextracted with EA
- washThe organic extracts are washed with water
- dry with materialdried (MgSO4)
- filtrationfiltered
- concentrationconcentrated
- customto give a crude residue
- dry with materialTrituration with hexane and drying in vacuo
Sources & evidence
- ORD record
- ord-699b66b986a64622bdda1b22511072bd
- Source dataset
- uspto-grants-1998_02
- Patent number
- US05714471
Reaction notes
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