HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1887131Generated: October 26, 2026
Potassium Carbonate → HCID 131730771, compound
https://huagongshe.com/reaction/1887131
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Pyridazine, 3-chloro-6-[4-(trifluoromethyl)phenyl]- | HCID 12449554 | — |
| Reactant | Piperidin-3-amine dihydrochloride | HCID 16211870 | — |
| Solvent | Acetone | HCID 180 | — |
| Product | HCID 131730771 | HCID 131730771 | 27.5% |
Reaction Steps
3-Chloro-6-(4-trifluoromethylphenyl)pyridazine (0.2 g, 0.77 mmol), 3-aminopiperidine dihydrochloride (0.27 g, 1.54 mmol) and potassium carbonate (0.53 g, 3.87 mmol) were mixed in acetone (4 mL) in a 20 mL microwave vessel. The reaction mixture was heated in a microwave oven for 2 h at 120° C. The reaction mixture was filtered and the precipitate was washed with MeOH. The combined organic phases were evaporated. The crude oil was purified on a silicagel column (0.04-0.063 mesh) using dichloromethane/MeOH (9:1) as eluent. This afforded 110 mg of a oil that was dissolved in MeOH and acidified with concentrated HCl (5 mL). The mixture was evaporated and the residue was dissolved in MeOH (1 mL) and ether (100 mL) was added with stirring. The mixture was evaporated to give 76 mg (25%) of the title compound as a yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08501739B2 |
|---|
| Source dataset | uspto-grants-2013_08 |
|---|
| ORD ID | ord-78955cab456448fc9a15d33d6b78631d |
|---|
| Source note | uspto-grants-2013_08 |
|---|