HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 968573Generated: October 29, 2026
2-(Tributylstannyl)pyridine → 7-pyridin-2-yl-3H-quinazolin-4-one
https://huagongshe.com/reaction/968573
Participants
| Role | Name | HCID | Charge |
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| Reactant | 2-(Tributylstannyl)pyridine | HCID 607784 | — |
| Reactant | 7-Bromo-3,4-dihydroquinazolin-4-one | HCID 135555612 | — |
| Catalyst | Tetrakis(triphenylphosphine)palladium | HCID 11979704 | — |
| Solvent | Dioxane toluene | HCID 21840791 | — |
| Product | 7-pyridin-2-yl-3H-quinazolin-4-one | HCID 135682059 | — |
Reaction Steps
To a solution of 7-bromo-3H-quinazolin-4-one (100 mg, 0.444 mmol) in toluene/dioxane (3:1), add 2-tributylstannanyl-pyridine (162 mg, 0.444 mmol) followed by tetrakis-(triphenylphosphine)-palladium(0) (26 mg, 0.022 mmol). Bubble dry nitrogen through the solution for 10 minutes then heat the stirring solution to 115° C. under a nitrogen atmosphere. After several minutes the reaction mixture becomes homogeneous. After 16 hours, cool the reaction vessel and collect the precipitate via filtration. Wash the solid with 25% EtOAc/hexanes followed by hexanes to give 7-pyridin-2-yl-3H-quinazolin-4-one as a beige solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07304059B2 |
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| Source dataset | uspto-grants-2007_12 |
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| ORD ID | ord-0e5e57aee81f4e3fb940b60b2a172e4e |
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| Source note | uspto-grants-2007_12 |
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