Calcium Acetate → N-benzyloxycarbonyl (beta-benzyl)-L-aspartyl-L-phenylalanine methyl ester
Reaction equation
C([O-])(=O)C.[Ca+2].C([O-])(=O)C.[CH2:10]([O:17][C:18]([NH:20][CH:21]([C:33](O)=[O:34])[CH:22]([CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:23]([OH:25])=[O:24])=[O:19])[C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1.[CH3:36][O:37][C:38](=[O:48])[C@H:39]([CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)[NH2:40].[OH-].[Na+]>CN(C)C=O>[CH3:36][O:37][C:38](=[O:48])[C@H:39]([CH2:41][C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1)[NH:40][C:33](=[O:34])[C@H:21]([CH:22]([CH2:26][C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1)[C:23](=[O:24])[OH:25])[NH:20][C:18]([O:17][CH2:10][C:11]1[CH:16]=[CH:15][CH:14]=[CH:13][CH:12]=1)=[O:19]Participants
Reactant 4
Product 1
Reagents, catalysts & solvents 1
Conditions
- Temperature
- 30 °C
Procedure
A 100 mg amount of Thermoase and 100 mg of an inhibitor for proteolytic enzyme obtained from the potato were admixed with 10 ml of tris-hydrochloric acid buffer solution (pH 8.0) containing 2.0 × 10-2M of calcium acetate. The mixture was stirred at 30° C. for 10 minutes. The insoluble material was removed by filtering the solution through a glass filter (G-3). The filtrate was mixed with 715 mg (2.00 mmol) of N-benzyloxycarbonyl-(β-benzyl)-D,L-aspartic acid and 215 mg (1.00 mmol) of L-phenylalanine methyl ester and then 1N NaOH was added to the filtrate to adjust the pH to 7.5. The reaction was carried out with stirring at 39° C. for 17 hours. The resulting white precipitate was treated in accordance with the process of Example 1 whereby 411 mg (yield of 79.2%) of N-benzyloxycarbonyl-(β-benzyl)-L-aspartyl-L-phenylalanine methyl ester having an [α]D23 = -12.5 (C=1.0 dimethylformamide)
Workup
- customA 100 mg amount of Thermoase and 100 mg of an inhibitor for proteolytic enzyme obtained from the potato
- customThe insoluble material was removed
- filtrationby filtering the solution through a glass
- filtrationfilter (G-3)
- stirringwith stirring at 39° C. for 17 hours
Sources & evidence
- ORD record
- ord-fb756444dd1349e497d7ea10fd2f21a9
- Source dataset
- uspto-grants-1978_09
- Patent number
- US04116768
Reaction notes
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