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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1514174Generated: November 4, 2026

Methyl iodide → 4-(Cyclohexylmethyl)-5-{2-[4-(2-methoxyphenyl)piperazino]ethyl}-2-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one

https://huagongshe.com/reaction/1514174

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethyl iodideHCID 6328—
Reactant2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amineHCID 3513851—
Reactant4-(cyclohexylmethyl)-5-{2-[4-(2-methoxyphenyl)piperazino]ethyl}-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 25184453—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product4-(Cyclohexylmethyl)-5-{2-[4-(2-methoxyphenyl)piperazino]ethyl}-2-methyl-2,4-dihydro-3H-1,2,4-triazol-3-oneHCID 2518479782.3%

Reaction Steps

To a slurry of PS-BEMP (0.95 g, 2.08 mmol, 2.2 mmol/g) and 4-(cyclohexylmethyl)-5-{2-[4-(2-methoxyphenyl)piperazino]ethyl}-2,4-dihydro-3H-1,2,4-triazol-3-one (E17; 415 mg, 1.028 mmol) in MeCN (20 mL), methyl iodide (0.13 mL, 2.08 mmol) was added and the reaction mixture was stirred at room temperature for 2 days. The resin was filtered, washed with MeOH (25 mL) and the solvent was evaporated in vacuo to afford 560 mg crude yellow glassy solid. This was dissolved in DCM (3 mL) and purified by flash chromatography (Flash Master, Biotage Isolute SI, 20 g column, gradient 0-10% MeOH in DCM over 30 min) to afford 350 mg of a light yellow oil. Further purification by preparative LC-MS afforded 190 mg (44%) of the title compound as a glassy solid.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08222254B2
Source datasetuspto-grants-2012_07
ORD IDord-2d3070c81b0a4519a514eb1cf5899f9a
Source noteuspto-grants-2012_07