HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 405990Generated: October 26, 2026
Potassium Carbonate → 2-(1-(6-methyl-4-oxo-3-phenyl-4H-pyrido[1,2-a]pyrimidin-2-yl)-ethyl)isoindoline-1,3-dione
https://huagongshe.com/reaction/405990
Participants
| Role | Name | HCID | Charge |
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| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Phenylboronic Acid | HCID 66827 | — |
| Reactant | 2-(1-(3-bromo-6-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-2-yl)ethyl)isoindoline-1,3-dione | HCID 66831340 | — |
| Catalyst | HCID 178478230 | HCID 178478230 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | 1,4-Dioxane | HCID 31275 | — |
| Product | 2-(1-(6-methyl-4-oxo-3-phenyl-4H-pyrido[1,2-a]pyrimidin-2-yl)-ethyl)isoindoline-1,3-dione | HCID 66831357 | — |
Reaction Steps
To a solution of phenylboronic acid (0.177 g, 1.45 mmol), 2-(1-(3-bromo-6-methyl-4-oxo-4H-pyrido[1,2-a]pyrimidin-2-yl)ethyl)isoindoline-1,3-dione (Prepared in Example 6, 0.40 g, 0.97 mmol) and potassium carbonate (0.402 g, 2.91 mmol) in a mixture of water (0.5 mL) and dioxane (9 mL) was added dichloro 1,1′-bis(diphenylphosphino)ferrocene palladium (II) (0.040 g, 0.049 mmol) under an argon atmosphere. The mixture was stirred at 90° C. for 3 h then was loaded onto silica gel and purified by MPLC (eluted with a gradient of 0-3% MeOH in DCM) to afford 2-(1-(6-methyl-4-oxo-3-phenyl-4H-pyrido[1,2-a]-pyrimidin-2-yl)ethyl)isoindoline-1,3-dione as a yellow solid. Mass Spectrum (ESI) m/e=410.1 (M+1).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08754089B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-27835a690963410ab4859fc17703a6d6 |
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| Source note | uspto-grants-2014_06 |
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