HuagongsheHuagongshe Chemistry Print Report · For research reference only
Butyl bromide → HCID 18695586, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Butyl bromide | HCID 8002 | — |
| Reactant | Potassium Fluoride | HCID 522689 | — |
| Reactant | HCID 69945232 | HCID 69945232 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 18695586 | HCID 18695586 | 69% |
Reaction Steps
To a suspension of N-(4-piperidyl)-1-n-propylindazole-3-carboxamide hydrochloride (0.52 g) obtained in Example 20 in acetonitrile were successively added 50% potassium fluoride--Celite (1.10 g) and 1-bromobutane (0.22 ml), and the mixture was heated under reflux for 11 hours. The reaction solution was filtered off, distilled off under reduced pressure, and to the residue was added chloroform and saturated aqueous sodium hydrogencarbonate. After extraction with chloroform, the chloroform layer was dried over anhydrous potassium carbonate, and distilled off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:methanol=20:1) to give the title compound (0.42 g) as a yellow oily substance. Yield=69%.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05945434 |
| Source dataset | uspto-grants-1999_08 |
| ORD ID | ord-79a0fb990f7d4dd18afb192911cf07b9 |
| Source note | uspto-grants-1999_08 |