Sodium Hydroxide → HCID 69545603, compound
Reaction equation
C[O:2][C:3](=[O:28])[C@H:4]([CH2:13][S:14][C:15]1[CH:20]=[CH:19][C:18]([C:21]([O:23][CH2:24][CH:25]=[CH2:26])=[O:22])=[CH:17][C:16]=1[NH2:27])[NH:5][C:6]([O:8][C:9]([CH3:12])([CH3:11])[CH3:10])=[O:7].[OH-].[Na+]>CC(OC)(C)C>[CH2:24]([O:23][C:21](=[O:22])[C:18]1[CH:19]=[CH:20][C:15]([S:14][CH2:13][C@@H:4]([NH:5][C:6]([O:8][C:9]([CH3:11])([CH3:10])[CH3:12])=[O:7])[C:3]([OH:28])=[O:2])=[C:16]([NH2:27])[CH:17]=1)[CH:25]=[CH2:26]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
200 mg (0.487 mmol) of N-tert-butoxycarbonyl-3-(4-alloxycarbonyl-2-aminophenylthio)-L-alanine methyl ester (96.7%) was added to a system consisting of 5 ml TBME and 20 ml buffer solution (0.1M sodium chloride; 3 mM sodium phosphate pH 7.0) under vigorous stirring. Enzyme [see following table] was added and the pH maintained at 7.0 under vigorous stirring by the controlled addition (pH-static) of 0.1N sodium hydroxide solution. The reaction was monitored by the consumption of titrating agent, and the formation of the product confirmed by HPLC.
Workup
- additionEnzyme [see following table] was added
- temperaturethe pH maintained at 7.0
- customThe reaction was monitored by the consumption
Sources & evidence
- ORD record
- ord-07580fbd379d4f88aeb87946cd3365d5
- Source dataset
- uspto-grants-2006_03
- Patent number
- US07011960B2
Reaction notes
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