HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 428444Generated: November 2, 2026
HCID 18358864, compound → HCID 23293563, compound
https://huagongshe.com/reaction/428444
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | HCID 18358864 | HCID 18358864 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | HCID 23293563 | HCID 23293563 | 51.6% |
Reaction Steps
A mixture of ethyl 3-phenyl-4-(4-chloro-2-aminobenzoyl)-1H-pyrazole-5-carboxylate (0.84 g, 2.28 mmol) and 2-hydroxypyridine (0.217 g, 2.28 mmol) in toluene (12 mL) was distilled at 160° C. until all the toluene was removed. The residue was heated at the same temperature for 18 hours. The reaction residue was washed with water to remove the 2-hydroxypyridine. The insoluble material was added to methanol (225 mL) and heated to boiling. Ethyl acetate (100 mL) was added and the solution heated for an additional 2 minutes, then concentrated to 100 mL. The solution was filtered to remove some insoluble material and the filtrate concentrated via rotovap until a precipitate formed which was filtered to give the title compound as a tan solid (0.381 g, 51%, mp 328.1-330.9° C.).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06313290B1 |
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| Source dataset | uspto-grants-2001_11 |
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| ORD ID | ord-65c415f67c904359afe698c9ffc33829 |
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| Source note | uspto-grants-2001_11 |
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