2,4-Dimethylbenzoyl chloride → HCID 59401817, compound
Reaction equation
[CH3:1][CH:2]1[CH2:6][CH2:5][CH2:4][N:3]1[CH:7]1[CH2:11][CH2:10][N:9]([C:12]2[CH:17]=[CH:16][C:15]([NH2:18])=[C:14]([C:19]([F:22])([F:21])[F:20])[CH:13]=2)[CH2:8]1.[CH3:23][C:24]1[CH:32]=[C:31]([CH3:33])[CH:30]=[CH:29][C:25]=1[C:26](Cl)=[O:27]>>[CH3:23][C:24]1[CH:32]=[C:31]([CH3:33])[CH:30]=[CH:29][C:25]=1[C:26]([NH:18][C:15]1[CH:16]=[CH:17][C:12]([N:9]2[CH2:10][CH2:11][CH:7]([N:3]3[CH2:4][CH2:5][CH2:6][CH:2]3[CH3:1])[CH2:8]2)=[CH:13][C:14]=1[C:19]([F:22])([F:20])[F:21])=[O:27]Participants
3
Procedure
The title compound was prepared in a manner substantially the same as example 1 by coupling 4-(2-methyl-[1,3′]bipyrrolidinyl-1′-yl)-2-trifluoromethyl-phenylamine with 2,4-dimethyl benzoyl chloride. MS: 446.2 (M+H).
Sources & evidence
- ORD record
- ord-1f3615eb7610475092d5dae3742023fd
- Source dataset
- uspto-grants-2013_12
- Patent number
- US08618159B2
Reaction notes
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