Reaction equation
[Br:1][C:2]1[S:6][C:5]([CH:7]([NH2:9])[CH3:8])=[CH:4][CH:3]=1.[CH3:10][O:11][C:12]([C:14]1[S:15][C:16]([C:19](O)=[O:20])=[CH:17][CH:18]=1)=[O:13]>>[CH3:10][O:11][C:12]([C:14]1[S:15][C:16]([C:19](=[O:20])[NH:9][CH:7]([C:5]2[S:6][C:2]([Br:1])=[CH:3][CH:4]=2)[CH3:8])=[CH:17][CH:18]=1)=[O:13]Participants
3
Procedure
The title compound was prepared in an analogous manner to that described in example 1, step 1 from 1-(5-bromo-thiophen-2-yl)-ethylamine and thiophene-2,5-dicarboxylic acid monomethyl ester.
Sources & evidence
- ORD record
- ord-403d778aa425413482b07f6a84b59747
- Source dataset
- uspto-grants-2008_07
- Patent number
- US07396944B2
Linked notes
Loading…