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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1694111Generated: November 1, 2026

Dimethylformamide → 5-[1,3]Dioxolan-2-yl-2-(pyridin-2-yloxymethyl)-pyridine

https://huagongshe.com/reaction/1694111

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethylformamideHCID 6228—
Reactant2-FluoropyridineHCID 9746—
ReactantSodium hydrideHCID 24758—
Reactant(5-[1,3]Dioxolan-2-yl-pyridin-2-yl)-methanolHCID 59255267—
SolventWaterHCID 962—
Product5-[1,3]Dioxolan-2-yl-2-(pyridin-2-yloxymethyl)-pyridineHCID 5925533877.3%

Reaction Conditions

Temperature0 °C

Reaction Steps

To an N,N-dimethylformamide (40 mL) solution of (5-[1,3]dioxolan-2-yl-pyridin-2-yl)-methanol (1.37 g, 7.56 mmol) described in Manufacturing Example 154-1-4 was added sodium hydride (333 mg, 8.32 mmol, 60% in oil), which was stirred for 5 minutes at 0° C. Next, 2-fluoropyridine (716 μL, 8.32 mmol) was added to the reaction mixture, which was stirred for 45 minutes at 50° C. Water was added to the reaction mixture at room temperature, which was extracted with ethyl acetate. The organic layer was separated, washed with water and saturated aqueous sodium chloride, dried over anhydrous magnesium sulfate, and filtered. The filtrate was concentrated under a reduced pressure, and the residue was purified by silica gel column chromatography (heptane:ethyl acetate=2:1 to 1:1) to obtain the title compound (1.51 g, 77%).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08158657B2
Source datasetuspto-grants-2012_04
ORD IDord-b132d8d8d47f49c09bc9547a4d3f8a35
Source noteuspto-grants-2012_04