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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

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantTriethylamineHCID 8471—
ReactantMethyl 6-chloro-5-fluoronicotinateHCID 12677297—
Reactant(R)-3-(2-ethoxyphenoxy)piperidineHCID 42553478—
SolventAcetonitrileHCID 6342—
Productmethyl (R)-6-(3-(2-ethoxyphenoxy)piperidin-1-yl)-5-fluoronicotinateHCID 13173707166.8%

Reaction Conditions

Temperature50 °C

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09440949B2
Source datasetuspto-grants-2016_09
ORD IDord-289fb72dd912409b99240efd16ec4903
Source noteuspto-grants-2016_09