HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Bromopyrimidine → (R)-2-(3-methylpiperazin-1-yl)pyrimidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Bromopyrimidine | HCID 78345 | — |
| Reactant | 2-Methylpiperazine, (R)- | HCID 7330434 | — |
| Solvent | O-Xylene | HCID 7237 | — |
| Product | (R)-2-(3-methylpiperazin-1-yl)pyrimidine | HCID 45099694 | 34% |
Reaction Steps
To a solution of (R)-2-methyl piperazine (4.0 g, 40 mmol) in xylene (100 mL) at 140° C. under nitrogen was added 2-bromo pyrimidine (6.36 g, 40 mmol) slowly over a period of 30 min. The heating was continued for additional 15 h and cooled. The solid precipitate was filtered and dried under suction and neutralized with a saturated aqueous solution of sodium bicarbonate. The product was extracted with DCM (2×50 mL), dried and evaporated to afford the title compound as a liquid (2.4 g, 34%). TLC-Chloroform/MeOH (8/2); Rf: 0.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08247437B2 |
| Source dataset | uspto-grants-2012_08 |
| ORD ID | ord-94d12ab267e3447092099ced46b3a4cb |
| Source note | uspto-grants-2012_08 |