HuagongsheHuagongshe Chemistry Print Report · For research reference only
t-Butyl (6-bromo-1,2,3,4-tetrahydro-8-nitro-3-quinolinyl)carbamate → t-Butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | t-Butyl (6-bromo-1,2,3,4-tetrahydro-8-nitro-3-quinolinyl)carbamate | HCID 15937762 | — |
| Reactant | HCID 178418361 | HCID 178418361 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | t-Butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate | HCID 19108500 | 103.3% |
Reaction Steps
A mixture of t-butyl (6-bromo-1,2,3,4-tetrahydro-8-nitro-3-quinolinyl)-carbamate (3.72 g, 0.01 mol), absolute ethanol (150 mL) and 10% palladium on carbon (0.60 g) was hydrogenated (50 lb hydrogen pressure) for 18 hours. The mixture was filtered through celite and the solvent removed. The residual foam was partitioned between ethyl acetate and 1 N sodium hydroxide, and the ethyl acetate phase was evaporated under reduced pressure to give 2.72 g of t-butyl (8-amino-1,2,3,4-tetrahydro-3-quinolyl)carbamate (compound XXXII) as an oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05436240 |
| Source dataset | uspto-grants-1995_07 |
| ORD ID | ord-99c56d5a397c4358b7817691392949c3 |
| Source note | uspto-grants-1995_07 |