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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 404392Generated: October 29, 2026

Thionyl Chloride → 4-(4-(Chloromethyl)-2-(1-vinylcyclopentyl)phenyl)-5-fluoro-2-methoxypyridine

https://huagongshe.com/reaction/404392

Reaction equation

Participants

RoleNameHCIDCharge
ReactantThionyl ChlorideHCID 24386—
Reactant(4-(5-Fluoro-2-methoxypyridin-4-yl)-3-(1-vinylcyclopentyl)phenyl)methanolHCID 57706064—
SolventDimethylformamideHCID 6228—
SolventDichloromethaneHCID 6344—
Product4-(4-(Chloromethyl)-2-(1-vinylcyclopentyl)phenyl)-5-fluoro-2-methoxypyridineHCID 57467656—

Reaction Steps

To a solution of (4-(5-fluoro-2-methoxypyridin-4-yl)-3-(1-vinylcyclopentyl)phenyl)methanol (47.0 mg, 144 μmol) in DMF (0.01 mL) and DCM (4.0 mL) was slowly added thionyl chloride (14.7 μL, 201 μmol) at 0° C. After addition, the resulting mixture was stirred at room temperature for 1 hour. The solvent was removed, and the product thus obtained was used in the next step without further purification. 1H NMR (400 MHz, CDCl3) δ ppm 8.01-8.11 (1H, m), 7.98 (1H, m), 7.47 (1H, s), 6.94 (1H, d, J=7.8 Hz), 6.69-6.82 (1H, m), 5.80 (1H, dd, J=17.2, 10.6 Hz), 4.89 (1H, d, J=10.2 Hz), 4.52-4.69 (3H, m), 3.89 (3H, s), 1.68-1.84 (4H, m), 1.49-1.67 (4H, m).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08748462B2
Source datasetuspto-grants-2014_06
ORD IDord-6ebe1200df6541508a6e88bee26d8b77
Source noteuspto-grants-2014_06