HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 705033Generated: October 30, 2026
Sodium → 2-{6-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]pyridin-2-yl}pyrimidine
https://huagongshe.com/reaction/705033
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium | HCID 5360545 | — |
| Reactant | 3-Azidopyridine | HCID 12066687 | — |
| Reactant | L-Ascorbic Acid | HCID 54670067 | — |
| Reactant | 2-(6-Ethynylpyridin-2-yl)pyrimidine | HCID 86698140 | — |
| Catalyst | Copper sulfate pentahydrate | HCID 24463 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | 2-{6-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]pyridin-2-yl}pyrimidine | HCID 67514358 | 10.4% |
Reaction Steps
100 mg (833 μmol) of 3-azidopyridine (for preparation see U.S. Pat. No. 4,775,762, CAUTION explosive!) and 151 mg (833 μmol) of 2-(6-ethynylpyridin-2-yl)pyrimidine were initially charged in a mixture of 1 ml of water and 1 ml of tert-butanol, 16.5 mg (83.3 μmol) of the sodium salt of L-ascorbic acid and 20.8 mg (83.3 μmol) of copper(II) sulfate pentahydrate were added, and the mixture was stirred at room temperature for 23 hours. The reaction mixture was then added to water and extracted repeatedly with dichloromethane. The separated organic phases were then dried over magnesium sulfate, filtered and concentrated. Chromatographic purification gave 26.0 mg (10% of theory) of 2-{6-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]pyridin-2-yl}pyrimidine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09173396B2 |
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| Source dataset | uspto-grants-2015_11 |
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| ORD ID | ord-705fe5ee5bb84c67af6bb44fce99981c |
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| Source note | uspto-grants-2015_11 |
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