HCID 53935835, compound → HCID 178462208, compound
Reaction equation
[CH2:1]([S:8][C:9]([NH:11][C@H:12]([C:14]([N:16]1[CH2:30][CH2:29][CH2:28][C@H:17]1[C:18]([N:20]1[CH2:27][CH2:26][CH2:25][C@H:21]1[C:22]([OH:24])=[O:23])=[O:19])=[O:15])[CH3:13])=[S:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.[NH2:31][C@H:32]([C:40]([OH:42])=[O:41])[CH2:33][CH2:34][CH2:35][NH:36][C:37](=[NH:39])[NH2:38]>O>[NH2:31][C@H:32]([C:40]([OH:42])=[O:41])[CH2:33][CH2:34][CH2:35][NH:36][C:37](=[NH:38])[NH2:39].[CH2:1]([S:8][C:9]([NH:11][C@H:12]([C:14]([N:16]1[CH2:30][CH2:29][CH2:28][C@H:17]1[C:18]([N:20]1[CH2:27][CH2:26][CH2:25][C@H:21]1[C:22]([OH:24])=[O:23])=[O:19])=[O:15])[CH3:13])=[S:10])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
N-(benzylthio)thiocarbonyl-L-alanyl-L-prolyl-L-proline (0.90 g, 2 m mole) was dissolved in L-arginine (0.35 g, 2 m mole) water (30 ml) solution, and the thus obtained solution was freeze-dried to give N-(benzylthio)thiocarbonyl-L-alanyl-L-prolyl-L-proline L-arginine salt (1.22 g).
Workup
- customthe thus obtained solution was freeze-dried
Sources & evidence
- ORD record
- ord-ac1f5638ffd246d58ad836a5efd0e63d
- Source dataset
- uspto-grants-1988_01
- Patent number
- US04719200
Reaction notes
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