HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2411234Generated: November 1, 2026
Ammonia → Tert-butyl 4-(5-cyano-3-methylpyridin-2-yl)piperazine-1-carboxylate
https://huagongshe.com/reaction/2411234
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ammonia | HCID 222 | — |
| Reactant | Water | HCID 962 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | tert-Butyl 4-(5-bromo-3-methylpyridin-2-yl)piperazine-1-carboxylate | HCID 46739269 | — |
| Catalyst | Zinc cyanide (Zn(CN)2) | HCID 11186 | — |
| Product | Tert-butyl 4-(5-cyano-3-methylpyridin-2-yl)piperazine-1-carboxylate | HCID 66838837 | — |
Reaction Steps
Under a nitrogen stream, 4-(5-bromo-3-methylpyridin-2-yl)piperazine-1-carboxylic acid tert-butyl ester (3.13 g) was dissolved in N,N-dimethylformamide (30 mL), zinc cyanide (1.03 g) and tetrakistriphenylphosphine palladium(0) (0.51 g) were added, and the mixture was stirred at 120° C. for 4 hr. After completion of the reaction, to the reaction mixture was added water/saturated aqueous ammonium chloride solution/28% aqueous ammonia (4:4:1), and the mixture was extracted with ethyl acetate. The organic layer was washed with water and saturated brine, and the solvent was evaporated. The obtained residue was purified by column chromatography (hexane:ethyl acetate) to give the title compound (2.46 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08816079B2 |
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| Source dataset | uspto-grants-2014_08 |
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| ORD ID | ord-9ef1defde2454c238f75db14c9933266 |
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| Source note | uspto-grants-2014_08 |
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