HuagongsheHuagongshe Chemistry Print Report · For research reference only
HCID 178526874, compound → HCID 178508078, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | HCID 178526874 | HCID 178526874 | — |
| Reactant | HCID 178526875 | HCID 178526875 | — |
| Product | HCID 178508078 | HCID 178508078 | — |
| Product | HCID 178508079 | HCID 178508079 | — |
Reaction Steps
In step (4) of Reaction Scheme V, a benzyloxy-3-nitroquinolin-4-ol or benzyloxy-3-nitro[1,5]naphthyridin-4-ol of Formula XLVI is reduced to provide a 3-amino-benzyloxyquinolin-4-ol or 3-aminobenzyloxy[1,5]naphthyridin-4-ol of Formula XLVII. The reaction can be carried out by hydrogenation using a heterogeneous hydrogenation catalyst such as platinum on carbon. The hydrogenation is conveniently carried out in a Parr apparatus in a suitable solvent such as dimethylformamide (DMF). The reaction can be carried out at ambient temperature, and the product or the hydrochloride salt thereof can be isolated using conventional methods.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08378102B2 |
| Source dataset | uspto-grants-2013_02 |
| ORD ID | ord-08fdadd3f27e456e81232df6f47f681d |
| Source note | uspto-grants-2013_02 |