HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 454861Generated: October 30, 2026
2,4-Difluoroaniline → HCID 45280130, compound
https://huagongshe.com/reaction/454861
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 2,4-Difluoroaniline | HCID 9709 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | HCID 46899466 | HCID 46899466 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | tert-Butanol | HCID 6386 | — |
| Product | HCID 45280130 | HCID 45280130 | — |
Reaction Steps
A mixture of 6-bromo-1-(2-methylpyrrolidin-1-yl)phthalazine (325 mg, 1.1 mmol), 2,4-difluorobenzenamine (287 mg, 2.2 mmol), Pd2(dba)3 (10.2 mg, 0.011 mmol), X-Phos (26.5 mg, 0.056 mmol), and potassium carbonate (384 mg, 2.8 mmol) in t-butanol (2.2 mL) was heated at 110° C. in an oil bath for 18 h. The mixture was cooled to RT, diluted with MeOH and filtered through a pad of Celite. The filtrate was concentrated. The resulting brown residue was purified by column chromatography (0-70% acetone in hexanes) to provide the title compound as a brown amorphous solid. MS (ESI, pos. ion) m/z: 341.2 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497269B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-ca376d91f01b4ef0ad7bfc4ce5b4b8e9 |
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| Source note | uspto-grants-2013_07 |
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