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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2257942Generated: November 2, 2026

2,4,6-Trimethylpyridine → HCID 22943405, compound

https://huagongshe.com/reaction/2257942

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
ReactantHCID 57194514HCID 57194514—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductHCID 22943405HCID 22943405—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of ethyl (3-amino-6-methyl-2-oxo-1,2-dihydropyridyl)acetate (0.55 g, 2.6 mmole) and 2,4,6-collidine (1.2 mL, 5.2 mmole) in tetrahydrofuran (10 mL) is cooled in an ice bath. A solution of benzylsulfonyl chloride (0.50 g, 2.6 mmole) in tetrahydrofuran (10 mL) is added over a 15 minute period. After addition is complete, the solution is stirred for 30 minutes at 0° C. The reaction mixture is diluted with ethyl acetate (100 mL), washed with 1.0N HCl (until aqueous layer is pH 1), water (10 mL), saturated sodium bicarbonate (10 mL), and brine (2×10 mL). The organic layer is dried over anhydrous magnesium sulfate, and the solvent is removed. The residue is chromatographed through silica gel using 0:100-20:80 ethyl acetate:dichloromethane as eluent to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05658930
Source datasetuspto-grants-1997_08
ORD IDord-3096ec9fc0a14644b02a13c94d0b4385
Source noteuspto-grants-1997_08