HuagongsheHuagongshe Chemistry Print Report · For research reference only
Benzyl 4-((tert-butoxycarbonyl)(methyl)amino)piperidine-1-carboxylate → 4-N-Boc-4-N-Methyl-aminopiperidine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Benzyl 4-((tert-butoxycarbonyl)(methyl)amino)piperidine-1-carboxylate | HCID 20782499 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Product | 4-N-Boc-4-N-Methyl-aminopiperidine | HCID 2756806 | — |
Reaction Steps
A mixture of 4-(tert-butoxycarbonyl-methyl-amino)-piperidine-1-carboxylic acid benzyl ester (17.5 mmol) and Pd—C (10%, 500 mg) in MeOH (150 mL) hydrogenated at atm. pressure and r.t. for 15 h. The mixture is filtered and evaporated. The residue is dissolved in CH2Cl2 (100 mL) and 1 M aq. NaOH (50 mL) is added. The mixture is stirred for 6 h at r.t., then the phases are separated and the aq. phase is extracted with CH2Cl2 (3×50 mL). The combined organic extracts are dried (Na2SO4), filtered and evaporated to provide the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07750161B2 |
| Source dataset | uspto-grants-2010_07 |
| ORD ID | ord-a68a6ca851604ecaaecb05539ba0318f |
| Source note | uspto-grants-2010_07 |