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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 849289Generated: October 31, 2026

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

https://huagongshe.com/reaction/849289

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 numberUS06011158
Source datasetuspto-grants-2000_01
ORD IDord-1bd1eb7820c044469b11a6a26f998080
Source noteuspto-grants-2000_01