HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → Benzyloxy-3-nitro[1,5]naphthyridin-4-amine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | Benzyloxy-4-chloro-3-nitroquinoline | HCID 21075762 | — |
| Reactant | Benzyloxy-4-chloro-3-nitro[1,5]naphthyridine | HCID 66650176 | — |
| Product | Benzyloxy-3-nitro[1,5]naphthyridin-4-amine | HCID 66649873 | — |
| Product | Benzyloxy-3-nitroquinolin-4-amine | HCID 66649911 | — |
Reaction Steps
In step (5) of Reaction Scheme V, a benzyloxy-4-chloro-3-nitroquinoline or benzyloxy-4-chloro-3-nitro[1,5]naphthyridine of Formula LV is treated with an amino alcohol of Formula XVI to provide a benzyloxy-3-nitroquinolin-4-amine or benzyloxy-3-nitro[1,5]naphthyridin-4-amine of Formula LVI. The reaction is conveniently carried out according to the methods described in step (1) of Reaction Scheme I.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08034938B2 |
| Source dataset | uspto-grants-2011_10 |
| ORD ID | ord-f2d629d9d5ed4d1c993b242d06211bc1 |
| Source note | uspto-grants-2011_10 |