HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 455686Generated: October 25, 2026
5-(Tributylstannyl)pyrimidine → 2-methoxy-7-(pyrimidin-5-yl)-9H-xanthen-9-one
https://huagongshe.com/reaction/455686
Participants
| Role | Name | HCID | Charge |
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| Reactant | 5-(Tributylstannyl)pyrimidine | HCID 2763249 | — |
| Reactant | 2-Dicyclohexylphosphino-2',4',6'-triisoprophylbiphenyl | HCID 11155794 | — |
| Reactant | 2-Bromo-7-methoxy-9H-xanthen-9-one | HCID 57475633 | — |
| Catalyst | Bis(dibenzylideneacetone)palladium | HCID 9811564 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-methoxy-7-(pyrimidin-5-yl)-9H-xanthen-9-one | HCID 57475654 | 60.2% |
Reaction Steps
A vial charged with Pd2(dba)3 (0.150 g, 0.164 mmol), XPhos (0.391 g, 0.819 mmol), 5-(tributylstannyl)pyrimidine (1.81 g, 4.92 mmol), 2-bromo-7-methoxy-9H-xanthen-9-one (1.000 g, 3.28 mmol) and dioxane (10 mL). The reaction mixture was evacuated and backfilled with nitrogen. The reaction mixture was heated to 100° C. overnight. The reaction mixture was cooled to RT and diluted with water and EtOAc. A grey solid precipitated out, which was filtered off. The solid was washed with EtOAc and water. The grey solid dried under reduced pressure to afford 2-methoxy-7-(pyrimidin-5-yl)-9H-xanthen-9-one) (0.600 g, 60.2% yield).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08497264B2 |
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| Source dataset | uspto-grants-2013_07 |
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| ORD ID | ord-7e96cc4aacfa414a9927a9d5c3bd74cc |
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| Source note | uspto-grants-2013_07 |
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