HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1915617Generated: October 25, 2026
Potassium Carbonate → 4-(4-amino-3-nitrophenoxy)-N-methylpicolinamide
https://huagongshe.com/reaction/1915617
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 4-Chloro-N-methylpicolinamide | HCID 1476814 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 4-Amino-3-Nitrophenol | HCID 3758882 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-amino-3-nitrophenoxy)-N-methylpicolinamide | HCID 17756497 | — |
Reaction Steps
A mixture containing 4-amino-3-nitrophenol (1 eq) and potassium bis(trimethylsilyl)amide (2 eq) was stirred in dimethylformamide for 2 hours at room temperature. To this mixture was added (4-chloro(2-pyridyl))-N-methylcarboxamide (1 eq) and potassium carbonate (1.2 eq) and stirred at 90° C. for 3 days. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered, and concentrated in vacuum to give brown solid. Purification on silica gel (2% triethyl amine/50% ethyl acetate in hexane) gave 4-[(4-amino-3-nitrophenyl)oxy]-N-methylpyridine-2-carboxamide as an orange solid. The product gave satisfactory NMR. HPLC, 3.39 min; MS: MH+=289.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08614330B2 |
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| Source dataset | uspto-grants-2013_12 |
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| ORD ID | ord-3e51a4f80d3b4c75b4885ecbaf067912 |
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| Source note | uspto-grants-2013_12 |
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