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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 397010Generated: October 28, 2026

2,4,6-Trimethylpyridine → Ethyl 5-benzylsulfonylamino-1-methoxymethyl-3-uracilylacetate

https://huagongshe.com/reaction/397010

Reaction equation

Participants

RoleNameHCIDCharge
Reactant2,4,6-TrimethylpyridineHCID 7953—
ReactantPhenylmethanesulfonyl chlorideHCID 74740—
ReactantEthyl 5-amino-1-methoxymethyluracilylacetateHCID 54496358—
SolventTetrahydrofuranHCID 8028—
SolventEthyl AcetateHCID 8857—
ProductEthyl 5-benzylsulfonylamino-1-methoxymethyl-3-uracilylacetateHCID 22943410—

Reaction Conditions

Temperature0 °C

Reaction Steps

A stirred solution of ethyl 5-amino-1-methoxymethyl-uracilylacetate (8.0 g, 31 mmole) and 2,4,6-collidine (13.7 mL, 62 mmole) in tetrahydrofuran (50 mL) is cooled in an ice bath. A solution of benzylsulfonyl chloride (5.93 g, 31 mmole) in tetrahydrofuran (50 mL) is added over a 30-minute period. After addition is complete, the solution is stirred for 1 hour at 0° C., then 3 hours at room temperature. The reaction mixture is diluted with ethyl acetate, washed with 1.0N HCl (until aqueous layer is pH 1), water, saturated sodium bicarbonate, and brine. The organic layer is dried over anhydrous magnesium sulfate, and the solvent is removed. The title compound is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06608204B1
Source datasetuspto-grants-2003_08
ORD IDord-83c86f7ff8e04d0fa620a4b2ef1ac2b7
Source noteuspto-grants-2003_08