HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258156Generated: November 2, 2026
Dichloromethane → 6-[1-(3-Trifluoromethyl-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile
https://huagongshe.com/reaction/1258156
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Dichloromethane | HCID 6344 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 1-{[3-(Trifluoromethyl)phenyl]methyl}piperidin-4-amine | HCID 12888929 | — |
| Reactant | 6-Chloropyridazine-3-carbonitrile | HCID 13382871 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | 6-[1-(3-Trifluoromethyl-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile | HCID 24989200 | 64% |
Reaction Steps
A mixture of 6-chloro-pyridazine-3-carbonitrile (D4) (0.130 g, 0.931 mmol), 1-(3-trifluoromethyl-benzyl)-piperidin-4-ylamine (D6) (0.241 g, 0.931 mmol) and diisopropylethylamine (0.243 ml, 1.4 mmol) in acetonitrile (3 ml) was stirred at 120° C. for 30 min., under microwave irradiation (Biotage MW-oven). Dichloromethane and water were added, and then the mixture washed with a saturated solution of sodium carbonate. The organic phase was filtered over cotton and the solvent was evaporated in vacuo. The residue was purified by column chromatography (silica gel; 0-2% ammonia in methanol (7M)/dichloromethane) to yield E16 (0.215 g, 64%) as a solid. C18H18F3N5 requires 361. Found 362 (MH+); mp: 170.3° C.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08466153B2 |
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| Source dataset | uspto-grants-2013_06 |
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| ORD ID | ord-f1c8b74b93d24522ab353a550e988c22 |
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| Source note | uspto-grants-2013_06 |
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