HCID 18369405, compound → HCID 54084756, compound

HRID 1699788Notes

Reaction equation

HRID 1699788 reaction equation
[F:1][C:2]1[CH:3]=[C:4]([C:10]2[C:15]([C:16]3[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([F:24])[CH:17]=3)=[N:14][NH:13][C:12](=[O:25])[CH:11]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9].[Cl:26][C:27]1[CH:36]=[CH:35][C:30]([CH:31]=[CH:32][CH2:33]Cl)=[CH:29][CH:28]=1>>[F:1][C:2]1[CH:3]=[C:4]([C:10]2[C:15]([C:16]3[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([F:24])[CH:17]=3)=[N:14][N:13]([CH2:33][CH:32]=[CH:31][C:30]3[CH:35]=[CH:36][C:27]([Cl:26])=[CH:28][CH:29]=3)[C:12](=[O:25])[CH:11]=2)[CH:5]=[CH:6][C:7]=1[O:8][CH3:9]

Participants

3

Reactant 2

HCID 18369405HCID 18369405, compoundHCID 53728250p-Chlorocinnamyl chloride

Product 1

HCID 54084756HCID 54084756, compoundYield 42.9%

Procedure

Using 5,6-bis(3-fluoro-4-methoxyphenyl)-2H-pyridazin-3-one and 4-chlorocinnamyl chloride as starting materials, the procedures of Example 12 were repeated likewise, whereby the title compound was obtained in a yield of 42.9%.

Sources & evidence

ORD record
ord-8cee894b8aef4ce184e47e2e1b5166c0
Source dataset
uspto-grants-2002_02
Patent number
US06348468B1

Reaction notes

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