HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1748658Generated: October 30, 2026
5-Bromonicotinamide → HCID 86692599, compound
https://huagongshe.com/reaction/1748658
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 5-Bromonicotinamide | HCID 1808 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Dimethylethylamine | HCID 11723 | — |
| Reactant | HCID 86692457 | HCID 86692457 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 86692599 | HCID 86692599 | 13.2% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09150555B2 |
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| Source dataset | uspto-grants-2015_10 |
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| ORD ID | ord-e15b4671fc7d41f3babb3d777d452c6f |
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| Source note | uspto-grants-2015_10 |
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