HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 534190Generated: October 31, 2026
2-Bromopyridine → Ethyl 2-(1-(pyridin-2-yl)piperidin-4-yl)acetate
https://huagongshe.com/reaction/534190
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-Bromopyridine | HCID 7973 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Piperidin-4-yl-acetic acid ethyl ester hydrochloride | HCID 45358839 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Ethyl 2-(1-(pyridin-2-yl)piperidin-4-yl)acetate | HCID 68385347 | 25.1% |
Reaction Steps
To a stirred solution of ethyl 2-(piperidin-4-yl)acetate, hydrochloride (2.0 g, 9.63 mmol) in DMF (40 mL) was added K2CO3 (3.99 g, 28.9 mmol) followed by 2-bromopyridine (1.521 g, 9.63 mmol) and stirred at 130° C. for 16 h. Reaction mixture was diluted with water (200 mL) and extracted with ethyl acetate (2×100 mL). The combined organic layer was washed with water (2×100 mL), brine (100 mL) and dried over Na2SO4 filtered and concentrated under reduced pressure. The residues was purified by column chromatography using 100-200 silica gel by eluting with 20% ethyl acetate in petroleum ether to afford ethyl 2-(1-(pyridin-2-yl)piperidin-4-yl)acetate (600 mg, 19.86% yield) as color less liquid. LCMS (ES) m/e 249.20 (M+H)+.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08853408B2 |
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| Source dataset | uspto-grants-2014_10 |
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| ORD ID | ord-5afc7cc2a0f8427694dda938d6077503 |
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| Source note | uspto-grants-2014_10 |
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