Ethyl 2-(2-aminothiazol-5-ylthio)acetate → {2-[3-((S)-2-Methoxy-1-methyl-ethoxy)-5-(3-methoxy-phenoxy)-benzoylamino]-thiazol-5-ylsulfanyl}-acetic Acid Ethyl Ester
Reaction equation
[CH3:1][O:2][CH2:3][C@H:4]([CH3:24])[O:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([O:15][C:16]2[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=2)[CH:14]=1)[C:9]([OH:11])=O.[CH2:25]([O:27][C:28](=[O:37])[CH2:29][S:30][C:31]1[S:35][C:34]([NH2:36])=[N:33][CH:32]=1)[CH3:26]>>[CH2:25]([O:27][C:28](=[O:37])[CH2:29][S:30][C:31]1[S:35][C:34]([NH:36][C:9](=[O:11])[C:8]2[CH:12]=[C:13]([O:15][C:16]3[CH:21]=[CH:20][CH:19]=[C:18]([O:22][CH3:23])[CH:17]=3)[CH:14]=[C:6]([O:5][C@@H:4]([CH3:24])[CH2:3][O:2][CH3:1])[CH:7]=2)=[N:33][CH:32]=1)[CH3:26]Participants
3
Procedure
The title compound was prepared from 3-((S)-2-methoxy-1-methyl-ethoxy)-5-(3-methoxy-phenoxy)-benzoic acid and (2-amino-thiazol-5-ylsulfanyl)-acetic acid ethyl ester following general procedure A
Sources & evidence
- ORD record
- ord-f6c944cd535a40e397f2123d7425d619
- Source dataset
- uspto-grants-2011_02
- DOI