3-Amino-1-methyl-5-phenyl-1H-benzo[E][1,4]diazepin-2(3H)-one → HCID 69284215, compound
Reaction equation
[NH2:1][CH:2]1[N:8]=[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)[C:6]2[CH:15]=[CH:16][CH:17]=[CH:18][C:5]=2[N:4]([CH3:19])[C:3]1=[O:20].[F:21][C:22]1[CH:23]=[C:24]([CH:34]=[C:35]([F:37])[CH:36]=1)[CH2:25][NH:26][C:27](=[O:33])[CH:28]([F:32])[C:29](O)=[O:30]>>[F:21][C:22]1[CH:23]=[C:24]([CH:34]=[C:35]([F:37])[CH:36]=1)[CH2:25][NH:26][C:27](=[O:33])[CH:28]([F:32])[C:29]([NH:1][CH:2]1[C:3](=[O:20])[N:4]([CH3:19])[C:5]2[CH:18]=[CH:17][CH:16]=[CH:15][C:6]=2[C:7]([C:9]2[CH:14]=[CH:13][CH:12]=[CH:11][CH:10]=2)=[N:8]1)=[O:30]Participants
3
Procedure
The title compound, MS: m/e=495.3 (M+H+), was prepared in analogy to example 16 from 3-amino-1,3-dihydro-1-methyl-5-phenyl-2H-1,4-benzodiazepin-2-one and N-(3,5-difluoro-benzyl)-2-fluoro-malonamic acid.
Sources & evidence
- ORD record
- ord-d089829498ef4bac88e6e19f3bfb2f1e
- Source dataset
- uspto-grants-2008_05
- Patent number
- US07375099B2
Reaction notes
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