HuagongsheHuagongshe Chemistry Print Report · For research reference only
Phosphorus oxybromide → 4-BroMo-1,6-naphthyridine
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Phosphorus oxybromide | HCID 24613 | — |
| Reactant | Phosphorus oxychloride | HCID 24813 | — |
| Reactant | HCID 178516446 | HCID 178516446 | — |
| Product | 4-BroMo-1,6-naphthyridine | HCID 12520142 | — |
| Product | 4-Chloro-1,6-naphthyridine | HCID 21766694 | — |
Reaction Steps
Paudler et al., J. Heterocyclic Chem. 2 (4), 393-8 (1965), show the synthesis and NMR spectra of various 4-substituted-1,6-naphthyridines, for example, the reaction of 4-hydroxy-1,6-naphthyridine with POBr3 or POCl3 to obtain 4-bromo-1,6-naphthyridine or 4-chloro-1,6-naphthyridine, respectively. Also shown is the reaction of 4-bromo-1,6-naphthyridine with dimethylamine to produce 4-dimethylamino-1,6-naphthyridine and the reaction 4-chloro-1,6-naphthyridine with piperidine or hydrazine to produce 4-(1-piperidinyl)-1,6-naphthyridine or 4-hydrazino-1,6-naphthyridine, respectively.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04634772 |
| Source dataset | uspto-grants-1987_01 |
| ORD ID | ord-7be1561bf12b419398ad66b2725c5a9b |
| Source note | uspto-grants-1987_01 |