HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazine → (R)-1-(4-Piperazin-1-yl-pyrimidin-2-yl)-ethyl acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | (R)-1-(4-methanesulfonyloxy-pyrimidin-2-yl)-ethyl acetate | HCID 54125954 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | (R)-1-(4-Piperazin-1-yl-pyrimidin-2-yl)-ethyl acetate | HCID 10922950 | 88% |
Reaction Steps
A mixture of (R)-1-(4-methanesulfonyloxy-pyrimidin-2-yl)-ethyl acetate (prepared according to the method of Preparation Six, 24.1 g, 92 mmol) and piperazine (16.0 g, 184 mmol) in tetrahydrofuran (200 mL) was heated at reflux for 1 h. This mixture was cooled, filtered, concentrated, and purified by flash column chromatography (9:1 dichloromethane/methanol) to give 24.4 g (88%) of the title compound as an oil. 1H NMR (CDCl3, 300 MHz) δ1.56 (d, 3H), 2.25 (s, 3H), 2.83 (m, 4H), 3.63 (m, 4H), 5.54 (q, 1H), 6.38 (d, 1H), 8.24 (d, 1H); MS (CI) 251 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06414149B1 |
| Source dataset | uspto-grants-2002_07 |
| ORD ID | ord-b9f7f1921bbb48e98a81873f448550ac |
| Source note | uspto-grants-2002_07 |