Isoamylamine → HCID 19926927, compound
Reaction equation
[C:1]([C:4]1[C:5](=[O:22])[NH:6][C:7]2[C:12]([C:13]=1C)=[C:11](OS(O)(=O)=O)[C:10]([F:20])=[CH:9][C:8]=2[Cl:21])(=[O:3])[CH3:2].[CH2:23]([NH2:28])[CH2:24][CH:25]([CH3:27])[CH3:26]>>[C:1]([C:4]1[C:5](=[O:22])[NH:6][C:7]2[C:12]([C:13]=1[NH:28][CH2:23][CH2:24][CH:25]([CH3:27])[CH3:26])=[CH:11][C:10]([F:20])=[CH:9][C:8]=2[Cl:21])(=[O:3])[CH3:2]Participants
3
Procedure
3-Acetyl-8-chloro-6-fluoro-4-methylsulfoxy-2-quinolinone (3.02g, 0.01 mol) and isoamylamine (0.87g, 0.01 mol) were used, but the reaction was carried out as the above process of example 37 to obtain the desired product (2.79g, yield: 86% ).
Sources & evidence
- ORD record
- ord-578e10fd77e34f62afa0f9e1057f61aa
- Source dataset
- uspto-grants-1995_07
- Patent number
- US05430153
Reaction notes
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