HCID 68819846, compound → HCID 59977272, compound
Reaction equation
C(O[C:5]1[CH:39]=[CH:38][CH:37]=[CH:36][C:6]=1[C:7]([NH:9][CH2:10][C@@H:11]([C:33]([OH:35])=[O:34])[NH:12][C:13](=[O:32])[C:14]1[CH:19]=[CH:18][C:17]([C:20]([NH:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([OH:30])[CH:25]=2)=[O:21])=[CH:16][C:15]=1[Cl:31])=[O:8])(=O)C.ClC1C=C(C(NCC2C=CC=C(O)C=2)=O)C=CC=1[C:43](N[C@H](C(O)=O)CNC(=O)C1C=CC(OCC)=CC=1)=[O:44].ClC1C=C(C(NCC2C=CC=C(O)C=2)=O)C=CC=1C(N[C@H](C(O)=O)CNC(=O)C1C=CC=CC=1OC)=O.ClC1C=C(C(NCC2C=CC=C(O)C=2)=O)C=CC=1C(N[C@H](C(O)=O)CNC(=O)C1C=CC(OC)=CC=1)=O.ClC1C=C(C(NCC2C=CC=C(O)C=2)=O)C=CC=1C(N[C@H](C(O)=O)CNC(=O)C1C=CC=C(C(OC)=O)C=1)=O.ClC1C=C(C(NCC2C=CC=C(O)C=2)=O)C=CC=1C(N[C@H](C(O)=O)CNC(=O)C1C=CC(OCCCCC)=CC=1)=O>>[Cl:31][C:15]1[CH:16]=[C:17]([C:20]([NH:22][CH2:23][C:24]2[CH:29]=[CH:28][CH:27]=[C:26]([OH:30])[CH:25]=2)=[O:21])[CH:18]=[CH:19][C:14]=1[C:13]([NH:12][C@H:11]([C:33]([OH:35])=[O:34])[CH2:10][NH:9][C:7](=[O:8])[C:6]1[CH:5]=[CH:39][CH:38]=[C:37]([O:44][CH3:43])[CH:36]=1)=[O:32]Participants
7
Procedure
3-(2-acetoxybenzoyl)amino-N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(4-ethoxybenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(2-methoxybenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(4-methoxybenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-[3-(methoxycarbonyl)benzoyl]amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(4-pentyloxybenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]aminolcarbonyl]benzoyl]-3-(3 ,4,5-trimethoxybenzoyl)amino-L-alanine;
Sources & evidence
- ORD record
- ord-ea31173ef2464d1082d15eef3bf02588
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331640B1
Reaction notes
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