HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1874611Generated: November 2, 2026
Potassium Carbonate → 5-bromo-N-{6-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy][1,2,4]triazolo[1,5-a]pyridin-2-yl}pyridine-3-carboxamide
https://huagongshe.com/reaction/1874611
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Oxalyl chloride | HCID 65578 | — |
| Reactant | 5-Bromonicotinic acid | HCID 88707 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | N-{3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-4-methylphenyl}-3-(1-cyano-1-methylethyl)benzamide | HCID 68985382 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Pyridine | HCID 1049 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | MeOH tetrahydrofuran | HCID 21899815 | — |
| Product | 5-bromo-N-{6-[5-({[3-(1-cyano-1-methylethyl)phenyl]carbonyl}amino)-2-methylphenoxy][1,2,4]triazolo[1,5-a]pyridin-2-yl}pyridine-3-carboxamide | HCID 57749198 | 86% |
Reaction Steps
To a solution of 5-bromopyridine-3-carboxylic acid (375 mg, 1.87 mmol) in tetrahydrofuran (6 mL) were added oxalyl chloride (204 μL, 2.34 mmol) and N,N-dimethylformamide (20 μL), and the mixture was stirred at room temperature for 1 hr. The reaction mixture was concentrated under reduced pressure. The obtained residue and N-{3-[(2-amino[1,2,4]triazolo[1,5-a]pyridin-6-yl)oxy]-4-methylphenyl}-3-(1-cyano-1-methylethyl)benzamide (400 mg, 0.937 mmol) were dissolved in pyridine (7 mL), and the mixture was stirred at room temperature for 1 hr. Water (15 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (15 mL, 5 mL). The combined organic layer was washed with saturated aqueous sodium hydrogen carbonate solution (3 mL) and saturated brine (2 mL), and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. To the obtained residue in methanol-tetrahydrofuran mixed solution (2:1, 6 mL) was added potassium carbonate (130 mg, 0.937 mmol), and the mixture was stirred at room temperature for 14 hr. A saturated aqueous sodium hydrogen carbonate solution (15 mL) was added to the reaction mixture, and the mixture was extracted with ethyl acetate (15 mL, 5 mL). The combined organic layer was washed with saturated brine (5 mL) and dried over anhydrous sodium sulfate. The insoluble material was filtered off, and the filtrate was concentrated under reduced pressure. The obtained residue was purified by silica gel column chromatography (NH silica gel, hexane/ethyl acetate=30/70→0/100), and fractions containing the desired product were concentrated under reduced pressure. Diisopropyl ether was added to the obtained residue. The obtained precipitate was collected by filtration and dried to give the title compound (490 mg, 86%) as a colorless powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08304557B2 |
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| Source dataset | uspto-grants-2012_11 |
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| ORD ID | ord-38d3515e60d6447ba44d0a2202e0455e |
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| Source note | uspto-grants-2012_11 |
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