2-Morpholin-4-yl-5-nitro-benzoyl chloride → HCID 59793629, compound
Reaction equation
[N:1]1([C:7]2[CH:15]=[CH:14][C:13]([N+:16]([O-:18])=[O:17])=[CH:12][C:8]=2[C:9](Cl)=[O:10])[CH2:6][CH2:5][O:4][CH2:3][CH2:2]1.[Cl:19][C:20]1[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:21]=1[N:27]1[CH2:32][CH2:31][NH:30][CH2:29][CH2:28]1>>[Cl:19][C:20]1[CH:25]=[C:24]([F:26])[CH:23]=[CH:22][C:21]=1[N:27]1[CH2:28][CH2:29][N:30]([C:9]([C:8]2[CH:12]=[C:13]([N+:16]([O-:18])=[O:17])[CH:14]=[CH:15][C:7]=2[N:1]2[CH2:6][CH2:5][O:4][CH2:3][CH2:2]2)=[O:10])[CH2:31][CH2:32]1Participants
3
Procedure
The title compound was prepared according to the procedure described for example 46 from 2-Morpholin-4-yl-5-nitro-benzoyl chloride and 1-(2-Chloro-4-fluoro-phenyl)-piperazine (70%, yellow solid, MS (m/e): 449.2 (M+H, 100%)
Sources & evidence
- ORD record
- ord-2a90e2e9172d477e8ead59cc879d26d3
- Source dataset
- uspto-grants-2008_09
- Patent number
- US07427612B2
Reaction notes
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