HuagongsheHuagongshe Chemistry Print Report · For research reference only
(R)-4-chloro-6-((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine → (R)-4((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | (R)-4-chloro-6-((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine | HCID 90411331 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | (R)-4((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine | HCID 90411653 | 99% |
Reaction Steps
(R)-4-chloro-6-((1-methylpiperidin-3-yl)oxy)pyrimidin-5-amine was dissolved in MeOH (15.0 mL) and Pd/C 10% (324.5 mg, 0.3049 mmol) was added and the reaction mixture stirred under a hydrogen atmosphere for 2 h. The reaction vessel was evacuated and flushed with nitrogen (3×), filtered through a celite pad washing with methanol followed by ethyl acetate. The combined filtrates were concentrated in vacuo to leave the title product 7a as a colourless oil (631 mg, 99%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08957078B2 |
| Source dataset | uspto-grants-2015_02 |
| ORD ID | ord-5811122b801a46ee9ccb51820b1fdb65 |
| Source note | uspto-grants-2015_02 |