HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 340486Generated: October 28, 2026
Potassium Carbonate → 6-(5-Nitropyridin-2-yl)-2-oxa-6-azaspiro[3.3]heptane
https://huagongshe.com/reaction/340486
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | N,N-dimethylformamide methanol | HCID 21901440 | — |
| Reactant | 2-Oxa-6-azaspiro[3.3]heptane | HCID 23111887 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-(5-Nitropyridin-2-yl)-2-oxa-6-azaspiro[3.3]heptane | HCID 68622075 | 54.9% |
Reaction Steps
Potassium carbonate (78 mg) and 2-oxa-6-azaspiro[3.3]heptane (30 mg) were added to a methanol/DMF (1 ml/2 ml) solution containing 2-chloro-5-nitropyridine (30 mg), followed by stirring at 80° C. for 3 hours. The reaction solution was adjusted to room temperature, and water was added, followed by extraction with ethyl acetate. The resultant was washed with saturated saline and dried over anhydrous sodium sulfate, the solvent was distilled away under reduced pressure, the obtained residue was purified by silica gel chromatography (n-hexane:ethyl acetate=1:1 to 1:4), and a white solid of 6-(5-nitropyridin-2-yl)-2-oxa-6-azaspiro[3.3]heptane (23 mg) was thus obtained.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08895585B2 |
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| Source dataset | uspto-grants-2014_11 |
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| ORD ID | ord-8e1d96e161e34dd9939da2f02031ad46 |
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| Source note | uspto-grants-2014_11 |
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