Benzyl Bromide → HCID 18369385, compound

HRID 1699787Notes

Reaction equation

HRID 1699787 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].[CH2:26](Br)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1>>[CH2:26]([N:13]1[C:12](=[O:25])[CH:11]=[C:10]([C:4]2[CH:5]=[CH:6][C:7]([O:8][CH3:9])=[C:2]([F:1])[CH:3]=2)[C:15]([C:16]2[CH:21]=[CH:20][C:19]([O:22][CH3:23])=[C:18]([F:24])[CH:17]=2)=[N:14]1)[C:27]1[CH:32]=[CH:31][CH:30]=[CH:29][CH:28]=1

Participants

3

Reactant 2

HCID 7498Benzyl BromideHCID 18369405HCID 18369405, compound

Product 1

HCID 18369385HCID 18369385, compoundYield 99.9%

Procedure

Using 5,6-bis(3-fluoro-4-methoxyphenyl)-2H-pyridazin-3-one and benzyl bromide as starting materials, the procedures of Example 12 were repeated likewise, whereby the title compound was obtained in a yield of 99.9%.

Sources & evidence

ORD record
ord-6175022623304641b493a5dcb6dc3b22
Source dataset
uspto-grants-2002_02
Patent number
US06348468B1

Reaction notes

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