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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 401490Generated: October 29, 2026

2-(Dimethylamino)ethanol → (6-Chloro-3-cyclopropylpyridin-2-yl)(2-fluoropyridin-3-yl)methanone

https://huagongshe.com/reaction/401490

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2-(Dimethylamino)ethanolHCID 7902—
Reactant2-Chloro-5-cyclopropylpyridineHCID 50988858—
Reactant2-Fluoro-N-methoxy-N-methylnicotinamideHCID 53417067—
ReactantButyllithiumHCID 178418339—
SolventTetrahydrofuranHCID 8028—
SolventHexaneHCID 8058—
Product(6-Chloro-3-cyclopropylpyridin-2-yl)(2-fluoropyridin-3-yl)methanoneHCID 5769052690.4%

Reaction Conditions

Temperature-78 °C

Reaction Steps

A 2.5M solution of nBuLi (10.94 ml, 27.34 mmol) was added to a solution of 2-(dimethylamino)ethanol (1.37 ml, 13.67 mmol) in hexane (15 ml) cooled to −78° C. The reaction mixture was stirred at −78° C. for 30 minutes then, a solution of 2-chloro-5-cyclopropylpyridine (700 mg, 4.56 mmol) in hexane (10 mL) was added dropwise. The reaction mixture was stirred for 90 minutes. A solution of 2-fluoro-N-methoxy-N-methylnicotinamide (3.36 g, 18.23 mmol) in tetrahydrofuran (15 mL) was added dropwise and the reaction mixture was stirred at −78° C. for 1 hour. The reaction mixture was partitioned between a saturated solution of ammonium chloride and ethyl acetate. The organic extract was washed with a saturated solution of sodium bicarbonate and brine, dried over magnesium sulfate, filtered and concentrated in vacuo. The residue was purified on silica gel by flash column chromatography to afford the title compound as a colourless oil (1.14 g, 61% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08741931B2
Source datasetuspto-grants-2014_06
ORD IDord-5c43ba88801a46089e4a9e6d6f7fe43f
Source noteuspto-grants-2014_06