HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1019694Generated: October 26, 2026
Potassium Carbonate → tert-butyl 2-(5'-bromo-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-4-yl)ethylcarbamate
https://huagongshe.com/reaction/1019694
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2,5-Dibromopyridine | HCID 69353 | — |
| Reactant | Sodium Bicarbonate | HCID 516892 | — |
| Reactant | 4-(2-Aminoethyl)piperidine, 4-BOC protected | HCID 1501849 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | tert-butyl 2-(5'-bromo-3,4,5,6-tetrahydro-2H-[1,2]bipyridinyl-4-yl)ethylcarbamate | HCID 66661183 | — |
Reaction Steps
10.37 g (43.80 mmol) of 2,5-dibromopyridine, 10.00 g (43.80 mmol) of tert-butyl 2-piperidin-4-ylethylcarbamate and 6.05 g (43.80 mmol) of potassium carbonate are placed in an autoclave. The mixture is then heated at 130° C. for 12 hours. The reaction mixture is allowed to cool to room temperature and then taken up in chloroform and saturated aqueous sodium hydrogen carbonate solution. The aqueous phase is separated out and extracted twice with chloroform, and the combined organic phases are washed with saturated aqueous sodium chloride solution and dried over sodium sulfate, and the filtrate is concentrated under reduced pressure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08716289B2 |
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| Source dataset | uspto-grants-2014_05 |
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| ORD ID | ord-dab2bd828e60411a9ec5e24385c50ac9 |
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| Source note | uspto-grants-2014_05 |
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