HCID 54173386, compound → HCID 68820374, compound

HRID 2270766Notes

Reaction equation

HRID 2270766 reaction equation
[Cl:1][C:2]1[CH:30]=[C:29]([C:31]([NH:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[C:37]([OH:41])[CH:36]=2)=[O:32])[CH:28]=[CH:27][C:3]=1[C:4]([NH:6][C@H:7]([C:24]([OH:26])=[O:25])[CH2:8][NH:9][C:10](=[O:23])[C:11]1[CH:16]=[C:15]([N+]([O-])=O)[CH:14]=[C:13]([N+]([O-])=O)[CH:12]=1)=[O:5].ClC1C=C(C(NCC2C=CC=C(O)C=2)=O)C=CC=1[C:45]([NH:47][C@H:48](C(O)=O)CNC(=O)C1C=CC=CC=1[N+]([O-])=O)=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([N+]([O-])=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([N+]([O-])=O)=CC=1)=O>>[Cl:1][C:2]1[CH:30]=[C:29]([C:31]([NH:33][CH2:34][C:35]2[CH:40]=[CH:39][CH:38]=[C:37]([OH:41])[CH:36]=2)=[O:32])[CH:28]=[CH:27][C:3]=1[C:4]([NH:6][C@H:7]([C:24]([OH:26])=[O:25])[CH2:8][NH:9][C:10](=[O:23])[C:11]1[CH:16]=[CH:15][C:14]([N:47]([CH3:48])[CH3:45])=[CH:13][CH:12]=1)=[O:5]

Participants

5

Reactant 4

HCID 54173386HCID 54173386, compoundHCID 68820792HCID 68820792, compoundHCID 68822969HCID 68822969, compoundHCID 86585141HCID 86585141, compound

Product 1

HCID 68820374HCID 68820374, compound

Procedure

N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]-amino]carbonyl]benzoyl]-3-(3,5-dinitrobenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(2-nitrobenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(3-nitrobenzoyl)amino-L-alanine; N-[2-chloro-4-[[[(3-hydroxyphenyl)methyl]amino]carbonyl]benzoyl]-3-(4-nitrobenzoyl)amino-L-alanine),

Sources & evidence

ORD record
ord-6757f5502a7a40b49902dd3f10177820
Source dataset
uspto-grants-2001_12
Patent number
US06331640B1

Reaction notes

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