HuagongsheHuagongshe Chemistry Print Report · For research reference only
8-(4-t-Butyloxycarbonylpiperazin-1-yl)quinoline → tert-Butyl 4-(1,2,3,4-tetrahydroquinolin-8-yl)piperazine-1-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 8-(4-t-Butyloxycarbonylpiperazin-1-yl)quinoline | HCID 15540678 | — |
| Catalyst | Platinum | HCID 23939 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | tert-Butyl 4-(1,2,3,4-tetrahydroquinolin-8-yl)piperazine-1-carboxylate | HCID 21070955 | 94.2% |
Reaction Steps
The compound of Step 2 (280 mg, 0.89 mmol) is dissolved in EtOH (70 mL), and Pt/C 10% (300 mg) is added. The mixture is pressurized to 45 psi under hydrogen and reacted for about 4 hours. The mixture is filtered over celite and concentrated. The residue is purified to afford about 266 mg of 8-(4-t-butyloxycarbonylpiperazin-1-yl)-1,2,3,4-tetrahydroquinoline (94%). EIS-MS 318.1 [M+1]
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07157463B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-ac3f519e8bfc47d78d906df483bba41c |
| Source note | uspto-grants-2007_01 |