Ethyl 2-(2-aminothiazol-5-ylthio)acetate → HCID 57776299, compound
Reaction equation
[CH:1]1([O:6][C:7]2[CH:8]=[C:9]([CH:13]=[C:14]([O:16][C:17]3[CH:22]=[CH:21][C:20]([F:23])=[CH:19][CH:18]=3)[CH:15]=2)[C:10](O)=[O:11])[CH2:5][CH2:4][CH2:3][CH2:2]1.[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:10](=[O:11])[C:9]2[CH:13]=[C:14]([O:16][C:17]3[CH:18]=[CH:19][C:20]([F:23])=[CH:21][CH:22]=3)[CH:15]=[C:7]([O:6][CH:1]3[CH2:5][CH2:4][CH2:3][CH2:2]3)[CH:8]=2)=[N:32][CH:31]=1)[CH3:25]Participants
3
Procedure
The title compound was prepared from 3-cyclopentyloxy-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-975ca23dfcb44cd092766862fa9d02dd
- Source dataset
- uspto-grants-2011_02
- Patent number
- US07880012B2
Reaction notes
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