Ethanol → HCID 86752918, compound
Reaction equation
[CH3:1][C:2]1[CH:3]=[C:4]([CH:20]=[C:21]([CH3:23])[CH:22]=1)[C:5]([N:7]([CH3:19])[C@@H:8]([C:16](O)=[O:17])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:6].[OH-].[Li+].C(O)C.Cl.C[O:31][C:32](=[O:43])[C@H:33]([CH2:35][CH2:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)[NH2:34]>CO.O>[CH3:1][C:2]1[CH:3]=[C:4]([CH:20]=[C:21]([CH3:23])[CH:22]=1)[C:5]([N:7]([CH3:19])[C@@H:8]([C:16]([NH:34][C@H:33]([C:32]([OH:31])=[O:43])[CH2:35][CH2:36][C:37]1[CH:42]=[CH:41][CH:40]=[CH:39][CH:38]=1)=[O:17])[CH2:9][C:10]1[CH:15]=[CH:14][CH:13]=[CH:12][CH:11]=1)=[O:6]Participants
6
Procedure
Coupling of N-(3,5-dimethylbenzoyl)-N-methyl-(D)-phenylalanine (derived from the corresponding methylester described in example 78 by hydrolysis with lithium hydroxide in methanol/water: [a]D =+88° (c=1.0, ethanol)) with (L)-homo-phenylalanine methyl ester hydrochloride according to example 1 followed by hydrolysis of the methyl ester moiety according to example 12 gives N-(3,5-dimethylbenzoyl)-N-methyl-(D)-phenylalanyl-(L)-homo-phenylalanine; FAB-MS m/e 473 (M+H)+.
Sources & evidence
- ORD record
- ord-c0721605975d4acfb5623a7c80dac504
- Source dataset
- uspto-grants-1998_07
- Patent number
- US05780498
Reaction notes
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