HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → HCID 9929493, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | 2-Bromo-4-methylpyridine | HCID 2734087 | — |
| Reactant | HCID 19018620 | HCID 19018620 | — |
| Reactant | HCID 19018651 | HCID 19018651 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Product | HCID 9929493 | HCID 9929493 | — |
Reaction Steps
g of 5,6-dihydro-2-methyl-1-[2-(piperazin-1-yl)-ethyl]-4H-pyrrolo[3,2,1-ij]quinoline, 1.45 g of 2-bromo-4-methylpyridine, 0.175 g of potassium iodide and 3 ml of triethylamine were heated at a temperature of 85° C. for 7 hours in 50 ml of dimethylformamide. The reaction mixture was worked up as described in Example 1H), and the crude title base obtained was converted into 5,6-dihydro-2-methyl-1-(2-[4-(4-methylpyridin-2-yl)piperazin-1-yl]ethyl}-4H-pyrrolo[3,2,1-ij]quinoline trihydrochloride having a melting point of 254° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05324725 |
| Source dataset | uspto-grants-1994_06 |
| ORD ID | ord-5684c560fa484afd9dde4fda03599d22 |
| Source note | uspto-grants-1994_06 |