HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 13499Generated: October 29, 2026
Potassium Carbonate → {4-[2-Methoxy-4-(methylamino)-5-nitrophenoxy] (2-pyridyl)}-n-methylcarboxamide
https://huagongshe.com/reaction/13499
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethylacetamide | HCID 31374 | — |
| Reactant | 3-chloro-N-methylbenzamide | HCID 4150792 | — |
| Reactant | 2-Methoxy-4-(methylamino)-5-nitrophenol | HCID 13742677 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Product | {4-[2-Methoxy-4-(methylamino)-5-nitrophenoxy] (2-pyridyl)}-n-methylcarboxamide | HCID 131725843 | — |
Reaction Steps
To a stirred solution of 2-methoxy-4-(methylamino)-5-nitrophenol (1 eq) in N,N-dimethylacetamide was added potassium-t-butoxide (1.2 eq) and continued stirring at ambient temperature utility solidified. To it was then added (3-chlorophenyl)-N-methylcarboxamide (1 eq) and anhydrous potassium carbonate (1 eq) and the resulting mixture was heated to 50° C. whereby the solid liquified. It was then heated to 110° C. for 12 h. After cooling to ambient temperature the solvent was distilled off and the resulting solid was extracted using ethyl acetate in a soxhlet apparatus for 48 h. The organic layer was cooled to 0° C., when the product crystallized from the ethyl acetate to give {4-[2-methoxy-4-(methylamino)-5-nitrophenoxy](2-pyridyl)}-N-methylcarboxamide. MS: MH+ 332
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-26afb6a5aec8481ca8746661fb2f0d69 |
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| Source note | uspto-grants-2010_06 |
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