HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1630472Generated: October 31, 2026
Diisopropylethylamine → HCID 59242655, compound
https://huagongshe.com/reaction/1630472
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Diisopropylethylamine | HCID 81531 | — |
| Reactant | 3,5-Difluorobenzyl bromide | HCID 518896 | — |
| Reactant | HCID 24880031 | HCID 24880031 | — |
| Solvent | Acetonitrile | HCID 6342 | — |
| Product | HCID 59242655 | HCID 59242655 | 53.2% |
Reaction Steps
A mixture of 4-phenyl-6-piperazin-1-yl-3-trifluoromethyl-pyridazine (E1) (0.050 g, 0.16 mmol), 3,5-difluorobenzyl bromide (0.031 ml, 0.24 mmol) and diisopropylethylamine (0.056 ml, 0.32 mmol) in acetonitrile (2 ml) was stirred at 100° C. for 10 min., under microwave irradiation. The solvent was evaporated in vacuo and then, dichloromethane and ammonium chloride (10% aqueous solution) were added. The mixture was filtered through a diatomaceous earth cartridge. The solvent was then evaporated in vacuo and the residue was purified by CC-TLC (centrifugal circular thin-layer chromatography) on a chromatotron (a preparative, centrifugally accelerated, radial, thin-layer chromatograph). The crude product was crystallised from diethyl ether/heptane to yield E3 (0.037 g, 52%) as a solid. C22H19F5N4 requires 434; Found 435 (MH+).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08791120B2 |
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| Source dataset | uspto-grants-2014_07 |
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| ORD ID | ord-14538d9e14e44d719055dadf3f7cab65 |
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| Source note | uspto-grants-2014_07 |
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