Phosphorus oxychloride → HCID 57454887, compound
Reaction equation
[Cl:1][C:2]1[CH:7]=[CH:6][C:5]([C:8]2[C:13]([CH3:14])=[N:12][NH:11][C:10](=O)[C:9]=2[C:16]2[N:17]=[N:18][C:19]([Cl:23])=[CH:20][C:21]=2[CH3:22])=[CH:4][CH:3]=1.P(Cl)(Cl)([Cl:26])=O>>[Cl:26][C:10]1[N:11]=[N:12][C:13]([CH3:14])=[C:8]([C:5]2[CH:6]=[CH:7][C:2]([Cl:1])=[CH:3][CH:4]=2)[C:9]=1[C:16]1[N:17]=[N:18][C:19]([Cl:23])=[CH:20][C:21]=1[CH3:22]Participants
Conditions
- Temperature
- 110 °C
Procedure
0.30 g of 5-(4-chlorophenyl)-4-(6-chloro-4-methyl-3-pyridazinyl)-6-met hyl-2H-pyridazin-3-one and 5 g of phosphorus oxychloride were mixed. The mixture was stirred for 1.5 hours on an oil bath of 110° C. The reaction mixture was allowed to cool to room temperature, the, concentrated under reduced pressure. To the resultant residue were added ethyl acetate and ice-cooled sodium bicarbonate water. The mixture was stirred for about 5 minutes at room temperature, then, liquid-separated. The organic layer was washed with brine, and dried over anhydrous magnesium sulfate, then, concentrated under reduced pressure. 0.31 g of the resultant residue was subjected to silica gel column chromatography, to obtain 0.26 g of 3-chloro-5-(4-chlorophenyl)-4-(6-chloro-4-methyl-3-pyridazin yl)-6-methylpyridazine (hereinafter, described as compound (13) of the present invention(13).).
Workup
- temperatureto cool to room temperature
- concentrationthe, concentrated under reduced pressure
- additionTo the resultant residue were added ethyl acetate and ice-
- temperaturecooled sodium bicarbonate water
- stirringThe mixture was stirred for about 5 minutes at room temperature
- customliquid-separated
- washThe organic layer was washed with brine
- dry with materialdried over anhydrous magnesium sulfate
- concentrationconcentrated under reduced pressure
Sources & evidence
- ORD record
- ord-e679c90297434e60943fcbf40841f16a
- Source dataset
- uspto-grants-2012_09
- Patent number
- US08258136B2
Reaction notes
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