7-Amino-5-methyl-5H-dibenzo[b,d]azepin-6(7H)-one → HCID 10480342, compound

HRID 2223288Notes

Reaction equation

HRID 2223288 reaction equation
[NH2:1][CH:2]1[C:8](=[O:9])[N:7]([CH3:10])[C:6]2[CH:11]=[CH:12][CH:13]=[CH:14][C:5]=2[C:4]2[CH:15]=[CH:16][CH:17]=[CH:18][C:3]1=2.[CH3:19][CH:20]([C:24]([NH:26][CH2:27][C:28]1[CH:33]=[C:32]([F:34])[CH:31]=[C:30]([F:35])[C:29]=1[F:36])=[O:25])[C:21](O)=[O:22]>>[CH3:19][CH:20]([C:24]([NH:26][CH2:27][C:28]1[CH:33]=[C:32]([F:34])[CH:31]=[C:30]([F:35])[C:29]=1[F:36])=[O:25])[C:21]([NH:1][CH:2]1[C:8](=[O:9])[N:7]([CH3:10])[C:6]2[CH:11]=[CH:12][CH:13]=[CH:14][C:5]=2[C:4]2[CH:15]=[CH:16][CH:17]=[CH:18][C:3]1=2)=[O:22]

Participants

3

Procedure

The title compound, MS: m/e=482.2 (M+H+), was prepared in analogy to example 16 from 7-amino-5-methyl-5H,7H-dibenzo[b,d]azepin-6-one and 2-methyl-N-(2,3,5-trifluoro-benzyl)-malonamic acid.

Sources & evidence

ORD record
ord-952c8f535f614474af92fc0b7391bafa
Source dataset
uspto-grants-2008_05
Patent number
US07375099B2

Reaction notes

Loading…