Reaction equation
[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1N=C=O.[NH2:9][C@H:10]([C:12]([NH:14][CH:15]1[N:21]=[C:20]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:19]2[CH:28]=[CH:29][CH:30]=[CH:31][C:18]=2[N:17]([CH3:32])[C:16]1=[O:33])=[O:13])[CH3:11]>>[S:1]1[CH:5]=[CH:4][CH:3]=[C:2]1[CH2:16][CH2:15][NH:14][C:12]([NH:9][C@H:10]([C:12]([NH:14][CH:15]1[N:21]=[C:20]([C:22]2[CH:27]=[CH:26][CH:25]=[CH:24][CH:23]=2)[C:19]2[CH:28]=[CH:29][CH:30]=[CH:31][C:18]=2[N:17]([CH3:32])[C:16]1=[O:33])=[O:13])[CH3:11])=[O:13]Participants
3
Procedure
Following General Procedure (5-A1) using 2-thiophene-yl isocyanate and 3-[(L-alaninyl)]amino-2,3-dihydro-1-methyl-5-phenyl-1H-1,4-benzodiazepin-2-one, as described in Example 8-B above, the title compound was prepared. The molecular weight as determined by mass spectrometry (FD) was: (M+H).
Sources & evidence
- ORD record
- ord-27f66d695ede4faa98323d6d95b1e560
- Source dataset
- uspto-grants-2003_05
- Patent number
- US06569851B1
Linked notes
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