HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2380929Generated: October 30, 2026
Phosphorus oxychloride → HCID 57447454, compound
https://huagongshe.com/reaction/2380929
Participants
| Role | Name | HCID | Charge |
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| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 57447459 | HCID 57447459 | — |
| Product | HCID 57447454 | HCID 57447454 | 69.7% |
Reaction Steps
0.3 g of 5-(4-chlorophenyl)-4-(5-chloro-3-fluoro-2-pyridyl)-6-methyl—2H-pyridazin-3-one and 10 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. 0.3 g of the resultant residue was subjected to silica gel column chromatography, to obtain 0.22 g of 3-chloro-5-(4-chlorophenyl)-4-(5-chloro-3-fluoro-2-pyridyl)-6-methylpyridazine (hereinafter, described as compound (14) of the present invention.).
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-9221323963024b7991e947deddb3ab32 |
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| Source note | uspto-grants-2012_09 |
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