Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 57776316, compound
Reaction equation
[F:1][C:2]1[CH:22]=[CH:21][C:5]([O:6][C:7]2[CH:8]=[C:9]([CH:13]=[C:14]([O:16][CH2:17][CH:18]([CH3:20])[CH3:19])[CH:15]=2)[C:10]([OH:12])=O)=[CH:4][CH:3]=1.[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:10](=[O:12])[C:9]2[CH:13]=[C:14]([O:16][CH2:17][CH:18]([CH3:20])[CH3:19])[CH:15]=[C:7]([O:6][C:5]3[CH:4]=[CH:3][C:2]([F:1])=[CH:22][CH:21]=3)[CH:8]=2)=[N:31][CH:30]=1)[CH3:24]Participants
3
Procedure
The title compound was prepared from 3-(4-fluoro-phenoxy)-5-isobutoxy-benzoic acid and (2-amino-thiazol-5-ylsulfanyl)-acetic acid ethyl ester following general procedure A
Sources & evidence
- ORD record
- ord-c62d3cb091f840939c1829697161f34b
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07880012B2
Reaction notes
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