HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1582862Generated: October 25, 2026
2-Fluoroethyl p-Toluenesulfonate → 1-Tert-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine
https://huagongshe.com/reaction/1582862
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2-Fluoroethyl p-Toluenesulfonate | HCID 256019 | — |
| Reactant | Tert-butyl 3-oxopiperazine-1-carboxylate | HCID 3157178 | — |
| Reactant | Potassium tert-butoxide | HCID 23665647 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 1-Tert-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine | HCID 22716468 | — |
Reaction Steps
1-t-Butoxycarbonyl-3-oxopiperazine (21.6 g) is dissolved in dry DMF (500 ml) and potassium t-butoxide (24.2 g) is added. The mixture is stirred at 20-25° for 30 minutes, then 1-(4-methylphenylsulfonyloxy)-2-fluoroethane (J. Med. Chem., 23(9), 985-90 (1980), 25.9 g) is added and stirring continued at the same temperature for 24 hours. The solvent is removed and the residue partitioned between ethyl acetate and water. The organic phase is washed with water and concentrated. The residue is dissolved in isopropanol and diluted with iso-hexane forming a precipitate which is removed by filtration. The mixture is chromatographed (silica; eluting with a gradient increasing in polarity from 0 to 50% isopropanol in iso-hexane) to give 1-t-butoxycarbonyl-4-(2-fluoroethyl)-3-oxopiperazine.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US06740652B2 |
|---|
| Source dataset | uspto-grants-2004_05 |
|---|
| ORD ID | ord-edc0064bb7804bc5a0816ac99c51519e |
|---|
| Source note | uspto-grants-2004_05 |
|---|