Diazomethane → 7-chloro-2-[[1-(methoxycarbonyl)-butylidene]hydrazino]-5-(o-chlorophenyl)-3H-1,4-benzodiazepine
Reaction equation
[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]=[C:10]([NH:12][N:13]=[C:14]([C:18]([OH:20])=[O:19])[CH2:15][CH2:16][CH3:17])[CH2:9][N:8]=[C:7]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[Cl:27])[C:6]=2[CH:28]=1.[N+](=[CH2:31])=[N-]>>[Cl:1][C:2]1[CH:3]=[CH:4][C:5]2[N:11]=[C:10]([NH:12][N:13]=[C:14]([C:18]([O:20][CH3:31])=[O:19])[CH2:15][CH2:16][CH3:17])[CH2:9][N:8]=[C:7]([C:21]3[CH:26]=[CH:25][CH:24]=[CH:23][C:22]=3[Cl:27])[C:6]=2[CH:28]=1Participants
3
Procedure
In the manner given in Example 10, a solution of 7-chloro-2-[(1-carboxybutylidene)hydrazino]-5-(o-chlorophenyl)-3H-1,4-benzodiazepine can be treated with ethereal diazomethane to give 7-chloro-2-[[1-(methoxycarbonyl)-butylidene]hydrazino]-5-(o-chlorophenyl)-3H-1,4-benzodiazepine.
Sources & evidence
- ORD record
- ord-179dff6213dd41f6bcb8ab1ccf5c40a9
- Source dataset
- uspto-grants-1977_04
- Patent number
- US04017492
Reaction notes
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