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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1609560Generated: October 30, 2026

Pyridine → Ethyl 5-chloromethyl-2,6-diisopropyl-4-(4-fluorophenyl)pyridine-3-carboxylate

https://huagongshe.com/reaction/1609560

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPyridineHCID 1049—
ReactantEthyl AcetateHCID 8857—
ReactantThionyl ChlorideHCID 24386—
ReactantEthyl 2,6-Diisopropyl-4-(4-fluorophenyl)-3-hydroxymethylpyridine-5-carboxylateHCID 10291957—
SolventTetrahydrofuranHCID 8028—
ProductEthyl 5-chloromethyl-2,6-diisopropyl-4-(4-fluorophenyl)pyridine-3-carboxylateHCID 20081869—

Reaction Steps

1.69 ml (20.9 mmol) of pyridine and 1.5 ml (20.9 mmol) of thionyl chloride are added successively at -5° C. to 5 g (13.9 mmol) of the compound from Example 4 dissolved in 100 m of dry tetrahydrofuran and the mixture is stirred for 15 minutes at the same temperature. The mixture is diluted using ethyl acetate and extracted several times using saturated sodium hydrogen carbonate solution, and the organic phases are dried over magnesium sulphate and concentrated in vacuo. The residue is chromatographed on a column (silica gel 70-230 mesh, in petroleum ether/ethyl acetate 95:5).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05401746
Source datasetuspto-grants-1995_03
ORD IDord-4e839dc3c52b47d2958fa378d41b1e8c
Source noteuspto-grants-1995_03