4-Fluoroaniline → HCID 86613125, compound
Reaction equation
[C:1](#[N:10])[CH:2]=[CH:3][C:4]1[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=1.[CH3:11][C:12]1[NH:16][N:15]=[C:14]([NH2:17])[CH:13]=1.[F:18][C:19]1[CH:25]=[CH:24][C:22]([NH2:23])=[CH:21][CH:20]=1>>[F:18][C:19]1[CH:25]=[CH:24][C:22]([NH:23][C:3]2[CH:2]=[C:1]([NH:17][C:14]3[CH:13]=[C:12]([CH3:11])[NH:16][N:15]=3)[N:10]=[C:1]([CH:2]=[CH:3][C:4]3[CH:9]=[CH:8][CH:7]=[CH:6][CH:5]=3)[N:10]=2)=[CH:21][CH:20]=1Participants
4
Procedure
Example 86 was synthesized via Scheme 6 according to the general scheme provided above with the appropriate starting materials cinnamonitrile, 5-methyl-1H-pyrazole-3-amine, and 4-fluoroaniline. Structure of the target was confirmed by 1H-NMR. The 1H-NMR is attached.
Workup
- customExample 86 was synthesized via Scheme 6 according to the general scheme
- customprovided above with the
Sources & evidence
- ORD record
- ord-01d759d4265d4e0d9ae345a791009fee
- Source dataset
- uspto-grants-2012_02
- Patent number
- US08114870B2
Reaction notes
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