HuagongsheHuagongshe Chemistry Print Report · For research reference only
4-Isobutyl-3-nitro quinoline → 4-Isobutyl 3-amino quinoline
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 4-Isobutyl-3-nitro quinoline | HCID 22590498 | — |
| Catalyst | Palladium | HCID 23938 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | 4-Isobutyl 3-amino quinoline | HCID 22590497 | — |
Reaction Steps
The nitroxide group on the 4-isobutyl-3-nitro quinoline produced in Example 1 is reduced by catalytic reduction using toluene as solvent, Pd/C 5% (50% wet) as catalyst, at 40–45° C. and atmospheric pressure to produce 4-isobutyl 3-amino quinoline. The rate of reaction depends on efficiency of stirring. After catalyst filtration the solution is ready for the next step.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07166721B2 |
| Source dataset | uspto-grants-2007_01 |
| ORD ID | ord-fb131e12f81d4c3eb6c8065d6a949e4f |
| Source note | uspto-grants-2007_01 |