Reaction equation
[Br:1][C:2]1[CH:3]=[C:4]([CH:8]([NH2:10])[CH3:9])[CH:5]=[CH:6][CH:7]=1.[CH3:11][O:12][C:13]([C:15]1[S:16][C:17]([C:20](O)=[O:21])=[CH:18][CH:19]=1)=[O:14]>>[CH3:11][O:12][C:13]([C:15]1[S:16][C:17]([C:20](=[O:21])[NH:10][CH:8]([C:4]2[CH:5]=[CH:6][CH:7]=[C:2]([Br:1])[CH:3]=2)[CH3:9])=[CH:18][CH:19]=1)=[O:14]Participants
3
Procedure
The title compound was prepared in an analogous manner to that described in example 1, step 1 from 1-(3-bromo-phenyl)-ethylamine and thiophene-2,5-dicarboxylic acid monomethyl ester.
Sources & evidence
- ORD record
- ord-a4dc2544990342118a0374a736339578
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07396944B2
Linked notes
Loading…