HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 59903Generated: October 30, 2026
Water → methyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinate
https://huagongshe.com/reaction/59903
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | Methyl 6-chloro-5-fluoronicotinate | HCID 12677297 | — |
| Reactant | (R)-3-(2-ethoxyphenoxy)piperidine | HCID 42553478 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | methyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinate | HCID 131737071 | 66.8% |
Reaction Steps
Triethylamine (0.45 mL, 3.3 mmol) was added to a stirred solution of (R)-3-(2-ethoxy-phenoxy)-piperidine (0.41 g, 1.6 mmol) and methyl 6-chloro-5-fluoronicotinate (0.30 g, 1.6 mmol) in acetonitrile (15 mL) at 0° C. The reaction mixture was heated at 50° C. for 18 h. The mixture was cooled to ambient temperature, water (30 mL) was added, and the mixture was extracted with ethyl acetate (3×50 mL). The combined organic layers were dried over sodium sulfate, filtered and concentrated. The crude material was purified by column chromatography (30% ethyl acetate-hexanes) to afford methyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinate (0.40 g). MS (ES+) 375.2 (M+H).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09440949B2 |
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| Source dataset | uspto-grants-2016_09 |
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| ORD ID | ord-289fb72dd912409b99240efd16ec4903 |
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| Source note | uspto-grants-2016_09 |
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