HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 32386Generated: October 29, 2026
Diisopropylethylamine → (5S)-5-({[4-(4-fluorophenyl)piperidin-1-yl}sulfonyl]methyl)-5-methylimidazolidine-2,4-dione
https://huagongshe.com/reaction/32386
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | (4S)-(4-methyl-2,5-dioxoimidazolidin-4-yl)methanesulphonyl chloride | HCID 16738713 | — |
| Reactant | 4-(4-Fluoro-phenyl)-piperidine hydrochloride | HCID 21898168 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (5S)-5-({[4-(4-fluorophenyl)piperidin-1-yl}sulfonyl]methyl)-5-methylimidazolidine-2,4-dione | HCID 59794371 | — |
Reaction Steps
4-(4-Fluorophenyl)piperidine hydrochloride (63 mg, 0.29 mmol) was taken up in 3 mL of dry THF, neutralized with diisopropylethylamine (50 μL, 0.29 mmol) and cooled on an ice-water bath. [(4S)-4-metyl-2,5-dioxo-imidazolodin-4-yl]methanesulfonyl chloride (80 mg, 0.35 mmol) was added and after stirring for 10 min, diisopropylethylamine (50 μL, 0.29 mmol) was added and the reaction mixture was stirred at ambient temperature until LC-MS (APCD) indicated consumption of the amine. The reaction mixture was evaporated and the residue taken up in EtOH and heated to 50° C. and allowed to cool before water was added. The precipitated product was collected and washed with EtOH/water and dried in vacuum to yield 87 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US07427631B2 |
|---|
| Source dataset | uspto-grants-2008_09 |
|---|
| ORD ID | ord-72cdafcdd2114a89a9df74afdb6ade70 |
|---|
| Source note | uspto-grants-2008_09 |
|---|