HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Tert-butyl[4-(2-methyl-2-oxiranylmethyl)piperazin-1-yl]carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Methyloxiran-2-ylmethyl paratoluenesulfonate | HCID 14237194 | — |
| Reactant | tert-Butyl piperazin-1-ylcarbamate | HCID 21701658 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | Tert-butyl[4-(2-methyl-2-oxiranylmethyl)piperazin-1-yl]carbamate | HCID 23081164 | 51.3% |
Reaction Steps
A mixture of (2-methyl-2-oxiranylmethyl) toluene-4-sufonate (9.75 g, 40.3 mmol), tert-butyl piperazin-1-yl-carbamate (6.75 g, 33.5 mmol) prepared in Reference Example 36, triethylamine (7 ml, 50.3 mmol) and potassium iodide (6.68 g, 33.5 mmol) in DMF (70 ml) was stirred at room temperature overnight. The reaction mixture was poured into water, and extracted with ethyl acetate. The extract was washed with water and brine, dried over sodium sulfate, and filtered. The filtrate was concentrated under reduced pressure. The residue was purified by silica gel column chromatography (hexane/acetone=4/1) to afford tert-butyl[4-(2-methyl-2-oxiranylmethyl)piperazin-1-yl]carbamate (4.66 g, yield 51%) as a colorless crystalline powder.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07262212B2 |
| Source dataset | uspto-grants-2007_08 |
| ORD ID | ord-22d6755f544d4a72960a99d739fd7135 |
| Source note | uspto-grants-2007_08 |