HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1258158Generated: November 1, 2026
Sodium Carbonate → 6-[1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile
https://huagongshe.com/reaction/1258158
Participants
| Role | Name | HCID | Charge |
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| Reactant | Sodium Carbonate | HCID 10340 | — |
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 6-Chloropyridazine-3-carbonitrile | HCID 13382871 | — |
| Reactant | 1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamine | HCID 53256189 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | 6-[1-(3,4,5-Trifluoro-benzyl)-piperidin-4-ylamino]-pyridazine-3-carbonitrile | HCID 24989201 | 74% |
Reaction Steps
A mixture of 6-chloro-pyridazine-3-carbonitrile (D4) (1.32 g, 9.46 mmol), 1-(3,4,5-trifluoro-benzyl)-piperidin-4-ylamine (D8) (2.10 g, 8.6 mmol) and diisopropylethylamine (2.25 ml, 12.9 mmol) in acetonitrile (12 ml) was stirred at 120° C. for 20 min., under microwave irradiation (Milestone MW-oven). Dichloromethane, water and a saturated solution of sodium carbonate were then added. The organic layers were filtered over cotton, evaporated in vacuo and the residue was purified by column chromatography (silica gel; 0-2% ammonia in methanol (7M)/dichloromethane). The desired fractions were collected and evaporated in vacuo. The residue was precipitated from diisopropyl ether to yield E18 (2.210 g, 74%) as a solid. C17H16F3N5 requires 347. Found 348 (MH+); mp: 185° 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-b37c9399d4f249f2a91a78c9019f2b47 |
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| Source note | uspto-grants-2013_06 |
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