Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 57776301, compound
Reaction equation
[C@H:1]([O:5][C:6]1[CH:7]=[C:8]([CH:12]=[C:13]([O:15][C:16]2[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=2)[CH:14]=1)[C:9]([OH:11])=O)([CH2:3][CH3:4])[CH3:2].[CH2:23]([O:25][C:26](=[O:35])[CH2:27][S:28][C:29]1[S:33][C:32]([NH2:34])=[N:31][CH:30]=1)[CH3:24]>>[CH2:23]([O:25][C:26](=[O:35])[CH2:27][S:28][C:29]1[S:33][C:32]([NH:34][C:9](=[O:11])[C:8]2[CH:12]=[C:13]([O:15][C:16]3[CH:21]=[CH:20][C:19]([F:22])=[CH:18][CH:17]=3)[CH:14]=[C:6]([O:5][C@@H:1]([CH2:3][CH3:4])[CH3:2])[CH:7]=2)=[N:31][CH:30]=1)[CH3:24]Participants
3
Procedure
The title compound was prepared from 3-((R)-sec-butoxy)-5-(4-fluoro-phenoxy)benzoic acid and (2-amino-thiazol-5-ylsulfanyl)-acetic acid ethyl ester following general procedure A
Sources & evidence
- ORD record
- ord-e3886838d21d413088b0c56a180d4b34
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07880012B2
Reaction notes
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