HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380923Generated: October 30, 2026
Phosphorus oxychloride → HCID 57503380, compound
https://huagongshe.com/reaction/2380923
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 57447448 | HCID 57447448 | — |
| Product | HCID 57503380 | HCID 57503380 | 72.1% |
Reaction Steps
0.64 g of 5-(4-chlorophenyl)-6-methyl-4-(2-pyrimidinyl)-2H-pyridazin-3-one and 10.4 g of phosphorus oxychloride were mixed. The mixture was stirred for 2 hours under reflux with heating. The reaction mixture was allowed to cool to room temperature, then, concentrated under reduced pressure. To the resultant residue was added ethyl acetate and ice-cooled sodium bicarbonate water was added. 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. 0.56 g of the resultant residue was subjected to silica gel column chromatography, to obtain 0.49 g of 3-chloro-5-(4-chlorophenyl)-6-methyl-4-(2-pyrimidinyl)pyridazine (hereinafter, described as compound (6) of the present invention(6).).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08258136B2 |
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| Source dataset | uspto-grants-2012_09 |
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| ORD ID | ord-7dc3bc70827a40f19e3a94dc08473d7c |
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| Source note | uspto-grants-2012_09 |
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