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) δ 1.56 (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 | US06936600B2 |
| Source dataset | uspto-grants-2005_08 |
| ORD ID | ord-6b025ade4bcb42e39fb12dd0c8eee653 |
| Source note | uspto-grants-2005_08 |