HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 64138Generated: October 29, 2026
Potassium Carbonate → N-(3-nitro-5-(2-oxopyridin-1(2H)-yl)phenyl)acetamide
https://huagongshe.com/reaction/64138
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N-(3-bromo-5-nitrophenyl)acetamide | HCID 10658908 | — |
| Reactant | HCID 178516071 | HCID 178516071 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | N-(3-nitro-5-(2-oxopyridin-1(2H)-yl)phenyl)acetamide | HCID 117777577 | 95% |
Reaction Steps
To a solution of N-(3-bromo-5-nitrophenyl)acetamide (1 g, 3.85 mmol), pyridin-2-ol (0.4 g, 4.24 mmol, 1.1 eq.), potassium carbonate (1 g, 1.3 mmol, 1.0 eq.) and copper(I) iodide (10 mg) in toluene (20 ml) was added trans cyclohexyl diamine (5 mg, 0.039 mmol, 0.01 eq.) and the mixture was heated at 100° C. for 16 h. The mixture was quenched and extracted as in Example 1(d). The solvent was distilled off and the residue was purified by column chromatography (60-120 silica gel, 50% ethyl acetate in hexane) to give the product in 95% yield (1 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09447091B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-3f289cb8667f4e2a94c23e7318ba3a20 |
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| Source note | uspto-grants-2016_09 |
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