HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1526336Generated: November 4, 2026
Phosphorus oxychloride → HCID 117770287, compound
https://huagongshe.com/reaction/1526336
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | HCID 117770222 | HCID 117770222 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 117770287 | HCID 117770287 | — |
Reaction Steps
Phosphorus oxychloride (2.59 mL) was slowly added to N,N-dimethylformamide (17.8 mL) under ice-cooling, and the mixture was stirred for 15 min. To the reaction mixture was added a solution of 1-(2-chlorophenyl)-4-hydroxy-6-methyl-2-oxo-1,2-dihydropyridine-3-carbonitrile obtained in Step D (2.90 g) in N,N-dimethylformamide (4.50 mL) under ice-cooling, and the reaction mixture was heated overnight at 80° C. The reaction mixture was cooled to room temperature, and poured into ice water, and the mixture was neutralized with saturated aqueous sodium hydrogen carbonate solution, and extracted with ethyl acetate. The extract was washed with water, and dried over anhydrous magnesium sulfate, and the solvent was evaporated under reduced pressure. The residue was recrystallized from ethyl acetate/hexane to give the title compound (2.50 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09085578B2 |
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| Source dataset | uspto-grants-2015_07 |
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| ORD ID | ord-42c97030dd854a77a824d07df79cde0b |
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| Source note | uspto-grants-2015_07 |
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