Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 57776285, compound
Reaction equation
[F:1][CH2:2][CH:3]([CH2:22][F:23])[O:4][C:5]1[CH:6]=[C:7]([CH:11]=[C:12]([O:14][C:15]2[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=2)[CH:13]=1)[C:8]([OH:10])=O.[CH2:24]([O:26][C:27](=[O:36])[CH2:28][S:29][C:30]1[S:34][C:33]([NH2:35])=[N:32][CH:31]=1)[CH3:25]>>[CH2:24]([O:26][C:27](=[O:36])[CH2:28][S:29][C:30]1[S:34][C:33]([NH:35][C:8](=[O:10])[C:7]2[CH:11]=[C:12]([O:14][C:15]3[CH:20]=[CH:19][C:18]([F:21])=[CH:17][CH:16]=3)[CH:13]=[C:5]([O:4][CH:3]([CH2:2][F:1])[CH2:22][F:23])[CH:6]=2)=[N:32][CH:31]=1)[CH3:25]Participants
3
Procedure
The title compound was prepared from 3-(2-fluoro-1-fluoromethyl-ethoxy)-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-f046ae5fe60843fba59aab703acea04a
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07880012B2
Reaction notes
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