HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-(1-Benzyl-4-methyl-piperidin-4-yl)-4-methyl-piperazine → 1-Methyl-4-(4-methylpiperidin-4-yl)piperazine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-(1-Benzyl-4-methyl-piperidin-4-yl)-4-methyl-piperazine | HCID 67272986 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 1-Methyl-4-(4-methylpiperidin-4-yl)piperazine | HCID 46738261 | — |
Reaction Steps
A suspension of 0.99 g (3.27 mmol) 1-(1-benzyl-4-methyl-piperidin-4-yl)-4-methyl-piperazine and 200 mg 10% Pd/C in 25 mL MeOH was hydrogenated at 50° C. and 50 psi hydrogen pressure for 2 h. To complete the reaction a further 200 mg catalyst were added and the reaction mixture was hydrogenated for a further 22 h at 60° C. and 50 psi hydrogen pressure. The catalyst was filtered off and the filtrate evaporated to dryness. The product was reacted further without purification.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07897603B2 |
| Source dataset | uspto-grants-2011_03 |
| ORD ID | ord-2e2719b399884ca1b6428ee2cb219ac4 |
| Source note | uspto-grants-2011_03 |