N-[2,6-dichloro-4-[[[(1R)-1-(1-naphthalenyl)ethyl]amino]carbonyl]benzoyl]-3-[(thiophene-2-carbonyl)amino]-L-alanine → 3-(1-butanesulfonyl)amino-N-[2-chloro-4-[[[(1R)-1-(1-naphthalenyl)ethyl]amino]carbonyl]benzoyl]-L-alanine

HRID 2270773Notes

Reaction equation

HRID 2270773 reaction equation
C(NC1S[C:7]([S:11]([NH:14][CH2:15][C@@H:16]([C:42]([OH:44])=[O:43])[NH:17][C:18](=[O:41])[C:19]2[CH:24]=[CH:23][C:22]([C:25]([NH:27][C@@H:28]([C:30]3[C:39]4[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=4)[CH:33]=[CH:32][CH:31]=3)[CH3:29])=[O:26])=[CH:21][C:20]=2[Cl:40])(=[O:13])=[O:12])=[C:8]([CH3:10])N=1)(=O)C.[CH3:45]C1C=C(C(N[C@@H](C2C3C(=CC=CC=3)C=CC=2)C)=O)C=C(C)C=1C(N[C@H](C(O)=O)CNC(C1SC=CC=1)=O)=O.BrC1C=C(C(N[C@@H](C2C3C(=CC=CC=3)C=CC=2)C)=O)C=CC=1C(N[C@H](C(O)=O)CNC(C1SC=CC=1)=O)=O.ClC1C=C(C(N[C@@H](C2C3C(=CC=CC=3)C=CC=2)C)=O)C=C(Cl)C=1C(N[C@H](C(O)=O)CNC(C1SC=CC=1)=O)=O>>[CH2:7]([S:11]([NH:14][CH2:15][C@@H:16]([C:42]([OH:44])=[O:43])[NH:17][C:18](=[O:41])[C:19]1[CH:24]=[CH:23][C:22]([C:25]([NH:27][C@@H:28]([C:30]2[C:39]3[C:34](=[CH:35][CH:36]=[CH:37][CH:38]=3)[CH:33]=[CH:32][CH:31]=2)[CH3:29])=[O:26])=[CH:21][C:20]=1[Cl:40])(=[O:12])=[O:13])[CH2:8][CH2:10][CH3:45]

Participants

5

Procedure

3-[(2-acetamido-4-methylthiazol-5-yl)sulfonyl]amino-N-[2-chloro-4-[[[(1R)-1-(1-naphthalenyl)ethyl]amino]carbonyl]benzoyl]-L-alanine; N-[2,6-dimethyl-4-[[[(1R)-1-(1-naphthalenyl)ethyl]amino]carbonyl]benzoyl]-3-(thiophene-2-carbonyl)amino-L-alanine; N-[2-bromo-4-[[[(1R)-1-(1-naphthalenyl)ethyl]amino]carbonyl]benzoyl]-3-(thiophene-2-carbonyl)amino-L-alanine), and N-[2,6-dichloro-4-[[[(1R)-1-(1-naphthalenyl)ethyl]amino]carbonyl]benzoyl]-3-[(thiophene-2-carbonyl)amino]-L-alanine;

Sources & evidence

ORD record
ord-55631affa3d24ac198cf89d98011ee18
Source dataset
uspto-grants-2001_12
Patent number
US06331640B1

Reaction notes

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