HCID 68821273, compound → HCID 68819682, compound
Reaction equation
NS(C1C=CC(C(NC[C@@H](C(O)=O)NC(=O)C2C=CC(C(NCC3C=CC=C(O)C=3)=O)=CC=2Cl)=O)=CC=1)(=O)=O.[Cl:40][C:41]1[CH:66]=[C:65]([C:67]([NH:69][CH2:70][C:71]2[CH:76]=[CH:75][CH:74]=[C:73]([OH:77])[CH:72]=2)=[O:68])[CH:64]=[CH:63][C:42]=1[C:43]([NH:45][C@H:46]([C:60]([OH:62])=[O:61])[CH2:47][NH:48][C:49](=[O:59])[C:50]1[CH:55]=[CH:54][CH:53]=[C:52]([N:56](C)C)[CH:51]=1)=[O:44]>>[NH2:56][C:52]1[CH:51]=[C:50]([CH:55]=[CH:54][CH:53]=1)[C:49]([NH:48][CH2:47][C@@H:46]([C:60]([OH:62])=[O:61])[NH:45][C:43](=[O:44])[C:42]1[CH:63]=[CH:64][C:65]([C:67]([NH:69][CH2:70][C:71]2[CH:76]=[CH:75][CH:74]=[C:73]([OH:77])[CH:72]=2)=[O:68])=[CH:66][C:41]=1[Cl:40])=[O:59]Participants
3
Procedure
3-(4-aminosulfonylbenzoyl)amino-N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(3-dimethylaminobenzoyl)amino-L-alanine;
Sources & evidence
- ORD record
- ord-c06375cd28c449b08561d81bd3b97e70
- Source dataset
- uspto-grants-2001_12
- Patent number
- US06331640B1
Reaction notes
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