HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258159Generated: November 1, 2026
Sodium Carbonate → 6-[1-(3,5-Difluoro-benzyl)-piperidin-4-ylamino]-4,5-dimethyl-pyridazine-3-carbonitrile
https://huagongshe.com/reaction/1258159
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-[(3,5-Difluorophenyl)methyl]piperidin-4-amine | HCID 22182400 | — |
| Reactant | 6-Chloro-4,5-dimethyl-pyridazine-3-carbonitrile | HCID 59253659 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-[1-(3,5-Difluoro-benzyl)-piperidin-4-ylamino]-4,5-dimethyl-pyridazine-3-carbonitrile | HCID 59253656 | 42% |
Reaction Steps
A mixture of 6-chloro-4,5-dimethyl-pyridazine-3-carbonitrile (D11) (0.120 g, 0.72 mmol), 1-(3,5-difluoro-benzyl)-piperidin-4-ylamine (D5) (0.194 g, 0.86 mmol) and diisopropylethylamine (0.188 ml, 1.08 mmol) in acetonitrile was stirred at 180° C. for 20 min., under microwave irradiation (Biotage MW-oven), and then again at 180° C. for additional 30 min. Dichloromethane, water and a saturated solution of sodium carbonate were then added. The organic phase was separated, filtered over cotton and evaporated in vacuo. The residue was purified by column chromatography (silica gel; 0-1% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and the solvent evaporated in vacuo to yield E19 (0.108 g, 42%) as a solid. C19H21F2N5 requires 357. Found 358 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| Patent number | US08466153B2 |
|---|
| Source dataset | uspto-grants-2013_06 |
|---|
| ORD ID | ord-d9fe36792021470db79704d6120dada9 |
|---|
| Source note | uspto-grants-2013_06 |
|---|