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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium CarbonateHCID 11430—
ReactantN,N-DimethylethylenediamineHCID 66053—
Reactantm-ToluamideHCID 69253—
Reactant3-[(1S)-1-azidoethyl]-5-bromopyridineHCID 86641860—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventEthyl AcetateHCID 8857—
Solvent1,4-DioxaneHCID 31275—
ProductN-{5-[(1S)-1-azidoethyl]pyridin-3-yl}-3-methylbenzamideHCID 8664186128.4%

Reaction Conditions

Temperature110 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08461161B2
Source datasetuspto-grants-2013_06
ORD IDord-943bdd80a1cf44b39ee5dad24f7fbcf5
Source noteuspto-grants-2013_06