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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methyl iodide | HCID 6328 | — |
| Reactant | 2-((1,1-Dimethylethyl)imino)-N,N-diethylhexahydro-1,3-dimethyl-2lambda5-1,3,2-diazaphosphorin-2-amine | HCID 3513851 | — |
| Reactant | 4-(cyclohexylmethyl)-5-{2-[4-(2-methoxyphenyl)piperazino]ethyl}-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 25184453 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 4-(Cyclohexylmethyl)-5-{2-[4-(2-methoxyphenyl)piperazino]ethyl}-2-methyl-2,4-dihydro-3H-1,2,4-triazol-3-one | HCID 25184797 | 82.3% |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08222254B2 |
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| Source dataset | uspto-grants-2012_07 |
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| ORD ID | ord-2d3070c81b0a4519a514eb1cf5899f9a |
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| Source note | uspto-grants-2012_07 |
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