HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1255841Generated: October 26, 2026
Potassium Carbonate → N-{5-[(1S)-1-azidoethyl]pyridin-3-yl}-3-methylbenzamide
https://huagongshe.com/reaction/1255841
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N,N-Dimethylethylenediamine | HCID 66053 | — |
| Reactant | m-Toluamide | HCID 69253 | — |
| Reactant | 3-[(1S)-1-azidoethyl]-5-bromopyridine | HCID 86641860 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | N-{5-[(1S)-1-azidoethyl]pyridin-3-yl}-3-methylbenzamide | HCID 86641861 | 28.4% |
Reaction Steps
A mixture of m-toluamide (164 mg, 1.21 mmol), 3-[(1S)-1-azidoethyl]-5-bromopyridine (227 mg, 1 mmol), copper (I) iodide (9.6 mg, 0.05 mmol), N,N-dimethylethylene diamine (0.011 mL, 0.1 mmol) and potassium carbonate (276 mg, 2 mmol) in dioxane (1 mL) was heated in a microwave reactor at 110° C. for 30 minutes then at 160° C. for a further 30 minutes. After this time the mixture was allowed to cool to room temperature, was diluted with ethyl acetate (5 mL) and was filtered through Celite. The filtrate was concentrated under reduced pressure to give a brown oil which was purified by flash chromatography (silica, ethyl acetate/dichloromethane) to give N-{5-[(1S)-1-azidoethyl]pyridin-3-yl}-3-methylbenzamide (80 mg, 28%) as a colourless oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08461161B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-943bdd80a1cf44b39ee5dad24f7fbcf5 |
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| Source note | uspto-grants-2013_06 |
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