HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 910692Generated: October 28, 2026
Cesium fluoride → HCID 57613225, compound
https://huagongshe.com/reaction/910692
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Cesium fluoride | HCID 25953 | — |
| Reactant | 2-(Di-tert-butylphosphino)biphenyl | HCID 2734215 | — |
| Reactant | 2-(Tri-n-butylstannyl)thiophene | HCID 2779373 | — |
| Reactant | 2-Chloro-6-(4-methylpiperazino)pyridine | HCID 10727230 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | HCID 57613225 | HCID 57613225 | — |
Reaction Steps
To a vial was added 1-(6-chloro-pyridin-2-yl)-4-methyl-piperazine (27 mg, 0.13 mmol), Pd2(dba)3 (14 mg), 2-(di-t-butylphosphino)biphenyl (18 mg), 2-thienyltributylstannane (51 mg, 0.15 mmol), dioxane (1 mL) and CsF (39 mg, 0.26 mmol). The resulting mixture was heated at 100° C. for 24 hrs. The resulting mixture was extracted with EtOAc. The organic layer was dried and concentrated, and the residue was purified by preparative TLC (hexanes/EtOAc) to yield the title compound as a solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022209B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-e84f367a4c514c37bf6b86f5ba7227bb |
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| Source note | uspto-grants-2011_09 |
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