Reaction equation
[N+:1]([C:4]1[CH:9]=[CH:8][C:7]([CH:10]([NH2:12])[CH3:11])=[CH:6][CH:5]=1)([O-:3])=[O:2].[CH3:13][O:14][C:15]([C:17]1[S:18][C:19]([C:22](O)=[O:23])=[CH:20][CH:21]=1)=[O:16]>>[CH3:13][O:14][C:15]([C:17]1[S:18][C:19]([C:22](=[O:23])[NH:12][CH:10]([C:7]2[CH:6]=[CH:5][C:4]([N+:1]([O-:3])=[O:2])=[CH:9][CH:8]=2)[CH3:11])=[CH:20][CH:21]=1)=[O:16]Participants
3
Procedure
The title compound was prepared in an analogous manner to that described in example 1, step 3 from 1-(4-nitro-phenyl)-ethylamine and thiophene-2,5-dicarboxylic acid monomethyl ester.
Sources & evidence
- ORD record
- ord-05f67a3f27674791aee08b5008da6f65
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07423060B2
Linked notes
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