3-Benzyl-6-chloro-4,5-dimethylpyridazine → 3-Chloro-6-(4-fluorobenzyl)-4,5-dimethylpyridazine
Reaction equation
[CH2:1]([C:8]1[N:9]=[N:10][C:11]([Cl:16])=[C:12]([CH3:15])[C:13]=1[CH3:14])[C:2]1[CH:7]=[CH:6][CH:5]=[CH:4][CH:3]=1.CC1(Cl)C(C)=CN(Cl)N=C1.[Br-].[F:28]C1C=CC(C[Zn+])=CC=1>>[Cl:16][C:11]1[N:10]=[N:9][C:8]([CH2:1][C:2]2[CH:3]=[CH:4][C:5]([F:28])=[CH:6][CH:7]=2)=[C:13]([CH3:14])[C:12]=1[CH3:15]Participants
4
Procedure
Analogous to compound 42 above, 3-chloro-6-(4-fluoro-benzyl)-4,5-dimethyl-pyridazine is prepared from 4,5-dimethyl-1,4-dichloro-pyridazine and para-fluoro benzyl zinc bromide.
Sources & evidence
- ORD record
- ord-257684ac2c9a430da9ee1801b583e811
- Source dataset
- uspto-grants-2016_08
- Patent number
- US09409871B2
Reaction notes
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