HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperidine → HCID 21814160, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperidine | HCID 8082 | — |
| Reactant | Hydrazine | HCID 9321 | — |
| Reactant | 4-Chloro-1,6-naphthyridine | HCID 21766694 | — |
| Product | HCID 21814160 | HCID 21814160 | — |
| Product | HCID 23270930 | HCID 23270930 | — |
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 | US04697021 |
| Source dataset | uspto-grants-1987_09 |
| ORD ID | ord-d6d1a0e729544c4e90fe865fb62e5618 |
| Source note | uspto-grants-1987_09 |