HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13522Generated: October 25, 2026
Potassium Carbonate → 4-(4-Amino-3-nitro-phenoxy)-pyridine-2-carboxylic acid dimethylamide
https://huagongshe.com/reaction/13522
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| Reactant | 4-Amino-3-Nitrophenol | HCID 3758882 | — |
| Reactant | 4-chloro-N,N-dimethylpyridine-2-carboxamide | HCID 4962252 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 4-(4-Amino-3-nitro-phenoxy)-pyridine-2-carboxylic acid dimethylamide | HCID 21037294 | — |
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-pyridine-2-carboxylic acid dimethylamide (1 eq) and potassium carbonate (1.2 eq) and then it was stirred at 90° C. for 3 days. The reaction mixture was then concentrated before partitioning between ethyl acetate and water. The organic layer was separated, washed with brine, dried, filtered and concentrated in vacuum to give brown solid. Purification by flash chromatography with ethyl acetate and hexane (1:1) gave the desired product as a yellow syrup. HPLC, 1.69 min; MS: MH+=303.1.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07728010B2 |
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| Source dataset | uspto-grants-2010_06 |
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| ORD ID | ord-2ce32362d15346048dc575b0b0923ee7 |
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| Source note | uspto-grants-2010_06 |
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