HuagongsheHuagongshe Chemistry Print Report · For research reference only
Sodium Iodide → HCID 70056084, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1,5-Dibromopentane | HCID 8100 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Methyl 1-(4-aminophenyl)-1H-pyrazole-4-carboxylate | HCID 57210789 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 70056084 | HCID 70056084 | — |
Reaction Steps
A solution of 1-(4-aminophenyl)-1H-pyrazol-4-carboxylic acid methyl ester (3.0 g) in N,N-dimethylformamide (30 ml) was treated with potassium carbonate (5.72 g), sodium iodide (4.14 g) and 1,5-dibromopentane, and the mixture was stirred for 20 hours at room temperature and 6 hours at 80° C., during which period additional N,N-dimethylformamide (20 ml), 1.5-dibromopentane (1.14 g) and potassium carbonate (0.95 g) were added. The reaction mixture was cooled to room temperature and poured into water. The precipitate was collected by filtration, dried over under reduced pressure. The residue was purified by silica gel chromatography (dichloromethane elution) to give 1-(4-piperidylphenyl)-1H-pyrazol-4-carboxylic acid methyl ester (1.34 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US06232290B1 |
| Source dataset | uspto-grants-2001_05 |
| ORD ID | ord-5f6656228171466682ef7eae85325d29 |
| Source note | uspto-grants-2001_05 |