HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 577540Generated: October 31, 2026
Potassium Carbonate → methyl 5-[(E)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethenyl]-2-(propan-2-yloxy)pyridine-4-carboxylate
https://huagongshe.com/reaction/577540
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 1H-Isoindole-1,3(2H)-dione, 2-ethenyl- | HCID 77035 | — |
| Reactant | Methyl 5-bromo-2-(propan-2-yloxy)pyridine-4-carboxylate | HCID 86723769 | — |
| Catalyst | HCID 178418851 | HCID 178418851 | — |
| Solvent | Toluene | HCID 1140 | — |
| Product | methyl 5-[(E)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethenyl]-2-(propan-2-yloxy)pyridine-4-carboxylate | HCID 86723770 | 34.3% |
Reaction Steps
To a solution of methyl 5-bromo-2-(propan-2-yloxy)pyridine-4-carboxylate (112a, 3.40 g, 12.4 mmol) and N-vinylphthalimide (2.58 g, 14.9 mmol) in toluene (124 mL) was added K2CO3 (5.19 g, 37.2 mmol) followed by Pd(P(tBu)3)2 (0.400 g, 0.775 mmol). The reaction mixture was degassed and heated in a sealed tube at 110° C. for 18 hours. The reaction mixture was cooled to room temperature and filtered through CELITE®. H2O (100 mL) was added, the organic layer was separated and concentrated under vacuum, and the residue was purified by column chromatography (0-80%, ethyl acetate/heptanes) to give methyl 5-[(E)-2-(1,3-dioxo-1,3-dihydro-2H-isoindol-2-yl)ethenyl]-2-(propan-2-yloxy)pyridine-4-carboxylate (112b, 1.56 g, 34%) as yellow solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US09040515B2 |
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| Source dataset | uspto-grants-2015_05 |
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| ORD ID | ord-6a1c3afdff394f9980b3d6a1b061bff8 |
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| Source note | uspto-grants-2015_05 |
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