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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantSodiumHCID 5360545—
Reactant3-AzidopyridineHCID 12066687—
ReactantL-Ascorbic AcidHCID 54670067—
Reactant2-(6-Ethynylpyridin-2-yl)pyrimidineHCID 86698140—
CatalystCopper sulfate pentahydrateHCID 24463—
SolventWaterHCID 962—
Solventtert-ButanolHCID 6386—
Product2-{6-[1-(pyridin-3-yl)-1H-1,2,3-triazol-4-yl]pyridin-2-yl}pyrimidineHCID 6751435810.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09173396B2
Source datasetuspto-grants-2015_11
ORD IDord-705fe5ee5bb84c67af6bb44fce99981c
Source noteuspto-grants-2015_11