HuagongsheHuagongshe Chemistry Print Report · For research reference only
N-(1-benzyl-4-piperidinyl)-N'-(4-fluorophenyl)urea → 283167-30-6
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | N-(1-benzyl-4-piperidinyl)-N'-(4-fluorophenyl)urea | HCID 6465310 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | 283167-30-6 | HCID 16781536 | 90.6% |
Reaction Steps
To a solution of N-(1-benzylpiperidin-4-yl)-N′-(4-fluorophenyl)urea (3.0 g) in a mixture of methanol (15 ml) and tetrahydrofuran (15 ml) was added palladium on carbon (10% w/w, 50% wet, 0.6 g), and the mixture was hydrogenated under atmospheric pressure of hydrogen for 8 hours. The catalyst was filtered off, and the solvents were evaporated under reduced pressure to give a residue, which was triturated with diisopropyl ether to give N-(piperidin-4-yl)-N′-(4-fluorophenyl)urea (1.97 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06710043B1 |
| Source dataset | uspto-grants-2004_03 |
| ORD ID | ord-0e0e635fb79f43279cfcdfadb65ec147 |
| Source note | uspto-grants-2004_03 |