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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1290652Generated: October 25, 2026

Potassium hydride → Dihydro-6-diethoxyphosphinyl-1-pyrindine-6-sulfonic acid, ethyl ester

https://huagongshe.com/reaction/1290652

Reaction equation

Participants

RoleNameHCIDCharge
ReactantPotassium hydrideHCID 82127—
ReactantEthyl (diethoxyphosphoryl)methanesulfonateHCID 10934205—
Reactant2,3-Bis(chloromethyl)pyridineHCID 14518750—
SolventDimethyl SulfoxideHCID 679—
ProductDihydro-6-diethoxyphosphinyl-1-pyrindine-6-sulfonic acid, ethyl esterHCID 86752567—

Reaction Conditions

Temperature90 °C

Reaction Steps

To an ice bath chilled solution of 35% potassium hydride in mineral oil (5.0 mmol) stirring under argon DMSO (7 ml) is added a solution of diethoxyphosphinyl methanesulfonic acid, ethyl ester (2.5 mmol) [prepared as described in J. C. Carretero, et. al., Tetrahedron, Vol. 43, pp. 5125-5134 (No. 21) 1987] in DMSO (5 ml). On completion of a dropwise addition, the resulting solution is stirred at room temperature for one hour. A solution of 2,3-bis(chloromethyl)pyridine (2.5 mmol) [prepared as described in K. Tsuda, et. al., Chem. Pharm. Bull., Vol.1, pp. 142, 1953] in DMSO (2 ml) is added slowly and the reaction mixture is then heated at 90° C. for 1 hour. After cooling, the reaction mixture is concentrated under reduced pressure and the desired product is purified by flash chromatography using a 5-15% isopropanol in methylene chloride gradient on silica gel.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05753634
Source datasetuspto-grants-1998_05
ORD IDord-230599ab80d54575b37403df5149cc58
Source noteuspto-grants-1998_05