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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 81655Generated: October 25, 2026

Cesium carbonate → 3-chloro-2-fluoro-5-[3-(tetrahydro-2H-pyran-2-yloxy)propoxy]pyridine

https://huagongshe.com/reaction/81655

Reaction equation

Participants

RoleNameHCIDCharge
ReactantCesium carbonateHCID 10796—
ReactantDimethylacetamideHCID 31374—
Reactant2-(3-Bromopropoxy)tetrahydro-2H-pyranHCID 2777988—
Reactant3-Chloro-2-fluoro-5-hydroxypyridineHCID 22451555—
SolventWaterHCID 962—
Product3-chloro-2-fluoro-5-[3-(tetrahydro-2H-pyran-2-yloxy)propoxy]pyridineHCID 6842976168%

Reaction Conditions

Temperature100 °C

Reaction Steps

2-(3-Bromopropoxy)tetrahydro-2H-pyran (12.93 g, 57.9 mmol) and cesium carbonate (39.5 g, 121.0 mmol) were added to an N,N-dimethylacetamide solution (80 ml) of 5-chloro-6-fluoropyridin-3-ol (8.14 g, 55.2 mmol), and stirred overnight under a nitrogen atmosphere at 100° C. The reaction solution was cooled with ice, water was added, and extracted with ethyl acetate. The organic layer was washed with water and saturated saline water, dried over anhydrous sodium sulfate, and concentrated under reduced pressure. The obtained residue was purified by amine-type silica gel column chromatography (Moritex NH, hexane:ethyl acetate=18:1 to 11:1) to obtain 3-chloro-2-fluoro-5-[3-(tetrahydro-2H-pyran-2-yloxy)propoxy]pyridine (10.84 g, yield: 68%) as a pale yellow oil.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846700B2
Source datasetuspto-grants-2014_09
ORD IDord-1b97044502834551b1bd9cd63cc5a8e0
Source noteuspto-grants-2014_09