HuagongsheHuagongshe Chemistry Print Report · For research reference only
1-Tert-butoxycarbonyl-4-(1-phenyl-1,2,3-triazol-4-yl)-1,2,3,6-tetrahydropyridine → tert-Butyl 4-(1-phenyl-1H-[1,2,3]triazol-4-yl)-piperidine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 1-Tert-butoxycarbonyl-4-(1-phenyl-1,2,3-triazol-4-yl)-1,2,3,6-tetrahydropyridine | HCID 19705292 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium hydroxide | HCID 9942167 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(1-phenyl-1H-[1,2,3]triazol-4-yl)-piperidine-1-carboxylate | HCID 54072376 | 99.4% |
Reaction Steps
tert-Butyl 4-[1-phenyl-1H-[1,2,3]triazol-4-yl]-1,2,3,6-tetrahydropyridine-1-carboxylate (5 mg) was dissolved in 1 ml of ethanol, a catalytic amount of 20% palladium hydroxide was added and the mixture was vigorously stirred for 30 minutes in a hydrogen atmosphere. The reaction solution was filtered through Celite. The solvent was evaporated from the resulting filtrate to give 5 mg of the title compound as a white solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07858800B2 |
| Source dataset | uspto-grants-2010_12 |
| ORD ID | ord-a4e806da0b1f4917a7aea25f4445f338 |
| Source note | uspto-grants-2010_12 |