HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019583Generated: October 31, 2026
Triethylamine → 2-(3-Azabicyclo[3.2.0]hept-3-yl)-5-nitropyridine
https://huagongshe.com/reaction/1019583
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Chloro-5-nitropyridine | HCID 78308 | — |
| Reactant | 3-Azabicyclo[3.2.0]heptane | HCID 21962587 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(3-Azabicyclo[3.2.0]hept-3-yl)-5-nitropyridine | HCID 66907896 | 87.6% |
Reaction Steps
A mixture of 0.1 g (0.63 mmol) of 2-chloro-5-nitropyridine, 0.1 g (0.75 mmol) of 3-aza-bicyclo[3.2.0]heptane (J. Med. Chem. 1967, 10(4), 621) and 0.26 mL (0.19 mmol) of triethylamine in 10 mL of dioxane, is heated at 65° C. for 4 h. The reaction mixture is then poured into 50 mL of ice water. The mixture is stirred until the ice has melted completely, then a yellow precipitate is collected by filtration and is dried at reduced pressure. In this way we isolate 0.121 g of the expected product in the form of a yellow powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716273B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-ce8f034158dc4b209a0686cef8599db9 |
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| Source note | uspto-grants-2014_05 |
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