HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 870452Generated: November 3, 2026
Acetic Anhydride → N-(4-((2-acetamidopyridin-4-yl)oxy)-2-chloro-5-fluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide
https://huagongshe.com/reaction/870452
Participants
| Role | Name | HCID | Charge |
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| Reactant | Acetic Anhydride | HCID 7918 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | N-(4-((2-aminopyridin-4-yl)oxy)-2-chloro-5-fluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide | HCID 73053629 | — |
| Product | N-(4-((2-acetamidopyridin-4-yl)oxy)-2-chloro-5-fluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide | HCID 73053670 | 50.5% |
Reaction Steps
To a solution of N-(4-((2-aminopyridin-4-yl)oxy)-2-chloro-5-fluorophenyl)-1,5-dimethyl-3-oxo-2-phenyl-2,3-dihydro-1H-pyrazole-4-carboxamide (200 mg, 0.43 mmol) in acetic anhydride (4 mL) was added Et3N (400 mg, 2.6 mmol). The mixture was stirred at 30° C. for 12 hours and concentrated in vacuo. The residue was purified by a silica gel column chromatography (DCM/CH3OH (v/v)=40/1) to give the title compound as a light yellow solid (110 mg, 50.5%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08969388B1 |
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| Source dataset | uspto-grants-2015_03 |
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| ORD ID | ord-b5f5106e79e64fd6849c0530664bbc5a |
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| Source note | uspto-grants-2015_03 |
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