HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1982397Generated: November 1, 2026
Methyl 2-anilinopyridine-3-carboxylate → 4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-one
https://huagongshe.com/reaction/1982397
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methyl 2-anilinopyridine-3-carboxylate | HCID 10998755 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Butyl Acetate | HCID 31272 | — |
| Product | 4-Hydroxy-1-phenyl-1,8-naphthyridin-2(1H)-one | HCID 54686473 | — |
Reaction Steps
To a stirred solution of 1 kg. of methyl 2-phenylamino-3-pyridine carboxylate in 3.97 liters of n-butyl acetate there is added portionwise, 1.1 kg. of potassium tertiary butoxide. After the addition of the potassium tertiary butoxide, there is added an additional 1.32 liters of n-butyl acetate. The reaction mixture is heated to reflux for 20 hours during which the internal temperature of the reaction mixture rises from 90° C. to 122° C. During this period, 1.8 liters of liquid is removed from the reaction via a Dean-Stark trap. Xylene (3.0 liters) is added to the reaction mixture and the remainder of the n-butyl acetate is removed via the Dean-Stark trap. The reaction mixture is cooled and the potassium salt is collected by filtration, washed with toluene and air dried. The crude potassium salt is dissolved in 12 liters of water, the aqueous solution is extracted with toluene, acidified to pH 2 and the product filtered and dried; weight 937 g., m.p. 311°-313° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04596809 |
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| Source dataset | uspto-grants-1986_06 |
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| ORD ID | ord-40dfd3586c1b4bff8ede258dfeb2b49e |
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| Source note | uspto-grants-1986_06 |
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