HuagongsheHuagongshe Chemistry Print Report · For research reference only
tert-Butyl (1-(2-chloropyrimidin-4-yl)piperidin-4-yl)carbamate → tert-Butyl (1-(pyrimidin-4-yl)piperidin-4-yl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | tert-Butyl (1-(2-chloropyrimidin-4-yl)piperidin-4-yl)carbamate | HCID 50742435 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Acetic Acid | HCID 176 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl (1-(pyrimidin-4-yl)piperidin-4-yl)carbamate | HCID 53426887 | — |
Reaction Steps
To a solution of 395 mg [1-(2-Chloro-pyrimidin-4-yl)-piperidin-4-yl]-carbamic acid tert-butyl ester in 10 mL ethanol and 0.3 mL acetic acid, 20 mg Pd/C (10%) were added and the mixture purged with argon for 10 min. Then the mixture was stirred under a hydrogen atmosphere for 5 h at RT. After addition of 10 mL ethyl acetate the reaction mixture was filtered through a pad of celite. The solvent was evaporated under reduced pressure and the residue codistilled twice with toluene to give the product as a white solid. Yield: 468 mg.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07741341B2 |
| Source dataset | uspto-grants-2010_06 |
| ORD ID | ord-6ba8c56a92e746c493d7340aee1b3076 |
| Source note | uspto-grants-2010_06 |