HuagongsheHuagongshe Chemistry Print Report · For research reference only
Hydroxylamine → 1h-Imidazo[4,5-c][1,5]naphthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Hydroxylamine | HCID 787 | — |
| Reactant | HCID 86625942 | HCID 86625942 | — |
| Reactant | HCID 86625943 | HCID 86625943 | — |
| Product | 1h-Imidazo[4,5-c][1,5]naphthyridine | HCID 178420735 | — |
Reaction Steps
In step (1) of Reaction Scheme VII, an N-(4-chloro[1,5]naphthyridin-3-yl)amide or N-(4-chloroquinolin-3-yl)amide of Formula XXXII is reacted with a hydroxylamine of the Formula Boc-CH2—X—CH2—ONH2 and cyclized to provide a 1H-imidazo[4,5-c][1,5]naphthyridine or a 1H-imidazo[4,5-c]quinoline of Formula LX. The reaction can be carried out using the method described in step (3) of Reaction Scheme I. Hydroxylamines of the Formula Boc-CH2—X—CH2—ONH2 can be prepared by conventional methods.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07579359B2 |
| Source dataset | uspto-grants-2009_08 |
| ORD ID | ord-b35a61f89b244ad58354c9f94795a88b |
| Source note | uspto-grants-2009_08 |