HuagongsheHuagongshe Chemistry Print Report · For research reference only
Piperazin-1-ylpropanol → 4-(3-hydroxypropyl)-N-(6-methoxy-4-methyl-8-quinolinyl)-1-piperazinehexanamide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Piperazin-1-ylpropanol | HCID 79207 | — |
| Reactant | 6-Bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamide | HCID 612023 | — |
| Solvent | Triethylamine | HCID 8471 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 4-(3-hydroxypropyl)-N-(6-methoxy-4-methyl-8-quinolinyl)-1-piperazinehexanamide | HCID 20207174 | 96% |
Reaction Steps
A mixture of 4.3 g (0.012 mole) of 6-bromo-N-(6-methoxy-4-methyl-8-quinolinyl)hexanamide and 3.5 g (0.024 mole) of 1-piperazinepropanol was heated at 120° for 2 hr and allowed to cool. The mixture was diluted with ethyl acetate and excess triethylamine, washed with water, dried over anhydrous magnesium sulfate, filtered and concentrated in vacuo to dryness to afford 4.9 g (96%) of the desired compound as a gum. The IR and NMR (CDCl3) were consistent with the assigned structure.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04659708 |
| Source dataset | uspto-grants-1987_04 |
| ORD ID | ord-d0fff633bbdf4e52882338496d65aa1e |
| Source note | uspto-grants-1987_04 |