Back
HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1775345Generated: November 1, 2026

Diethyl chlorophosphate → 1-(Diethoxyphosphorylmethylsulfonyl)-4-(4-methyl-2-pyridyl)piperazine

https://huagongshe.com/reaction/1775345

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDiethyl chlorophosphateHCID 13139—
ReactantAmmonium ChlorideHCID 25517—
ReactantLithium HexamethyldisilazideHCID 2733832—
Reactant1-(4-Methyl-2-pyridinyl)-4-(methylsulfonyl)piperazineHCID 89826010—
SolventTetrahydrofuranHCID 8028—
Product1-(Diethoxyphosphorylmethylsulfonyl)-4-(4-methyl-2-pyridyl)piperazineHCID 8982580481.1%

Reaction Conditions

Temperature-78 °C

Reaction Steps

1-(4-Methyl-2-pyridyl)-4-methylsulfonyl-piperazine (1.16 g, 4.54 mmol) was dissolved in anhydrous THF (80 ml) and cooled under nitrogen to −78° C. Lithium bis(trimethylsilyl)amide (1M in THF, 14 ml, 14 mmol) was added dropwise and the mixture was stirred at −78° C. for one hour. Diethyl chlorophosphate (3.1 g, 18 mmol) was added dropwise and stirring was continued for one hour at −78° C., after which the mixture was allowed to reach room temperature over three hours. A saturated solution of ammonium chloride was added and the mixture was extracted with DCM (3×), the combined organic layers were dried (sodium sulfate), concentrated under reduced pressure and the residue was purified by column chromatography (silica, gradient from 0 to 6% methanol in DCM) to give 1.44 g of a light-brown oil (3.68 mmol, yield 81%) MS (ESI) m/z=392.1 [M+1]+.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS09260441B2
Source datasetuspto-grants-2016_02
ORD IDord-d3f1ae9dd82148ec9c7f3ef99e994bfc
Source noteuspto-grants-2016_02