HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1454980Generated: October 30, 2026
7-bromo-1-(2,6-difluorophenyl)-2H-quinolizin-2-one → 7-(2,4-difluorobenzyl)-1-(2,6-difluorophenyl)-2H-quinolizin-2-one
https://huagongshe.com/reaction/1454980
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | 7-bromo-1-(2,6-difluorophenyl)-2H-quinolizin-2-one | HCID 57531230 | — |
| Reactant | HCID 178505768 | HCID 178505768 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 7-(2,4-difluorobenzyl)-1-(2,6-difluorophenyl)-2H-quinolizin-2-one | HCID 16749633 | — |
Reaction Steps
To a solution of 7-bromo-1-(2,6-difluorophenyl)-2H-quinolizin-2-one (100 mg, 0.3 mmole) was added 2,4-difluorobenzylzincbromide (0.5 N in THF, 1.2 ml), and tetrakis (15 mg) in THF. The mixture was heated to 90° C. until reaction complete. The mixture was diluted with ethyl acetate, washed with 1N HCl, brine and dried over MgSO4. Upon concentration, the mixture was purified by gel chromatography (100% ethyl acetate) to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07482345B2 |
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| Source dataset | uspto-grants-2009_01 |
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| ORD ID | ord-ac211283edc340bf8f0682882680f728 |
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| Source note | uspto-grants-2009_01 |
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