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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748658Generated: October 30, 2026

5-Bromonicotinamide → HCID 86692599, compound

https://huagongshe.com/reaction/1748658

Reaction equation

Participants

RoleNameHCIDCharge
Reactant5-BromonicotinamideHCID 1808—
ReactantPotassium CarbonateHCID 11430—
ReactantDimethylethylamineHCID 11723—
ReactantHCID 86692457HCID 86692457—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventWaterHCID 962—
Solvent1,4-DioxaneHCID 31275—
ProductHCID 86692599HCID 8669259913.2%

Reaction Conditions

Temperature100 °C

Reaction Steps

A solution of 5-bromopyridine-3-carboxamide (734 mg), 8-(5-bromopyridin-2-yl)-1,4-dioxaspiro[4.5]decane-8-carbonitrile (1.18 g) described in Reference Example 82, copper (I) iodide (35 mg), N,N-dimethylethylamine (33 mg) and potassium carbonate (1.01 g) in 1,4-dioxane (5 ml) was stirred at 100° C. for six hours. After completion of the reaction, water was added and extracted with ethyl acetate. The organic layer was dried over anhydrous magnesium sulfate and concentrated. The residue was purified with column chromatography to give 5-bromo-N-[6-(8-cyano-1,4-dioxaspiro[4.5]dec-8-yl)pyridin-3-yl]nicotinamide (213 mg).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09150555B2
Source datasetuspto-grants-2015_10
ORD IDord-e15b4671fc7d41f3babb3d777d452c6f
Source noteuspto-grants-2015_10