HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1800470Generated: November 1, 2026
Potassium Carbonate → 3-(1-cyano-1-methylethyl)-N-{4-ethyl-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide
https://huagongshe.com/reaction/1800470
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | 3-(1-cyano-1-methylethyl)-N-(4-ethyl-3-hydroxyphenyl)benzamide | HCID 68419192 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 3-(1-cyano-1-methylethyl)-N-{4-ethyl-3-[(5-nitropyridin-2-yl)oxy]phenyl}benzamide | HCID 68420119 | 118.3% |
Reaction Steps
To a solution of 2-chloro-5-nitropyridine (1.07 g, 6.81 mmol) and 3-(1-cyano-1-methylethyl)-N-(4-ethyl-3-hydroxyphenyl)benzamide (2.0 g, 6.48 mmol) in N,N-dimethylformamide (15 mL) was added potassium carbonate (1.34 g, 9.72 mmol), and the mixture was stirred at 80° C. for 12 hr. The reaction mixture was cooled to room temperature, the insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was diluted with ethyl acetate (200 mL), washed with water (150 mL), 5% aqueous sodium hydrogen carbonate solution (150 mL) and saturated brine (150 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, the filtrate was concentrated under reduced pressure, and the obtained residue was purified by silica gel column chromatography (hexane/ethyl acetate=80/20→30/70). The obtained solution was concentrated under reduced pressure to give the title compound (3.3 g, quantitative) as a yellow amorphous substance.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08344135B2 |
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| Source dataset | uspto-grants-2013_01 |
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| ORD ID | ord-e175a5698015498d85e62e65f602ef7e |
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| Source note | uspto-grants-2013_01 |
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