Benzylamine → HCID 19957198, compound
Reaction equation
[C:1]([NH:4][CH:5]1[CH2:9][CH2:8][N:7]([C:10]2[CH:19]=[C:18]3[C:13]([C:14](=[O:38])[C:15]([C:33]([O:35][CH2:36][CH3:37])=[O:34])=[CH:16][N:17]3[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[O:26][CH2:27][O:28][CH2:29][CH2:30][O:31][CH3:32])=[C:12](F)[C:11]=2[F:40])[CH2:6]1)(=[O:3])[CH3:2].[CH2:41]([NH2:48])[C:42]1[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=1>>[C:1]([NH:4][CH:5]1[CH2:9][CH2:8][N:7]([C:10]2[CH:19]=[C:18]3[C:13]([C:14](=[O:38])[C:15]([C:33]([O:35][CH2:36][CH3:37])=[O:34])=[CH:16][N:17]3[C:20]3[CH:25]=[CH:24][CH:23]=[CH:22][C:21]=3[O:26][CH2:27][O:28][CH2:29][CH2:30][O:31][CH3:32])=[C:12]([NH:48][CH2:41][C:42]3[CH:47]=[CH:46][CH:45]=[CH:44][CH:43]=3)[C:11]=2[F:40])[CH2:6]1)(=[O:3])[CH3:2]Participants
3
Procedure
Ethyl 7-(3-acetamidopyrrolidin-1-yl)-5,6-difluoro-1-(2-methoxyethoxymethoxyphenyl)-4-oxo-4H-quinoline-3-carboxylate is reacted with benzylamine by a procedure similar to that of Example 22 step 3 to prepare the title compound.
Sources & evidence
- ORD record
- ord-b052d397631f419e8e5546dda3c154b7
- Source dataset
- uspto-grants-1994_06
- Patent number
- US05318965
Reaction notes
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