Reaction equation
[CH:1]([C:4]1[CH:25]=[CH:24][CH:23]=[CH:22][C:5]=1[O:6][C:7]1[CH:21]=[CH:20][C:10]([CH:11]=[C:12]2[S:16][C:15](SC)=[N:14][C:13]2=[O:19])=[CH:9][CH:8]=1)([CH3:3])[CH3:2].[NH:26]1[CH2:29][CH:28]([C:30]([OH:32])=[O:31])[CH2:27]1>CN(C=O)C>[CH:1]([C:4]1[CH:25]=[CH:24][CH:23]=[CH:22][C:5]=1[O:6][C:7]1[CH:21]=[CH:20][C:10]([CH:11]=[C:12]2[S:16][C:15]([N:26]3[CH2:29][CH:28]([C:30]([OH:32])=[O:31])[CH2:27]3)=[N:14][C:13]2=[O:19])=[CH:9][CH:8]=1)([CH3:3])[CH3:2]Participants
4
Reactant 2
Product 1
Reagents, catalysts & solvents 1
Procedure
was prepared from 5-[4-(2-Isopropyl-phenoxy)-benzylidene]-2-methylsulfanyl-thiazol-4-one and azetidine-3-carboxylic acid and substituting MeCN with DMF as described in Example 5C
Sources & evidence
- ORD record
- ord-0a181029bd3b42d4bbd01523928417cf
- Source dataset
- uspto-grants-2013_11
- Patent number
- US08580832B2
Linked notes
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