HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1820892Generated: October 26, 2026
Ethyl Acetate → 4-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine
https://huagongshe.com/reaction/1820892
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | 1H-Pyrrolo(2,3-b)pyridine | HCID 9222 | — |
| Reactant | 3,4-Dimethoxyphenylboronic acid | HCID 2734702 | — |
| Reactant | 4-Chloro-1H-pyrrolo[2,3-b]pyridine | HCID 11389493 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Solvent | Potassium Carbonate | HCID 11430 | — |
| Product | 4-(3,4-Dimethoxy-phenyl)-1H-pyrrolo[2,3-b]pyridine | HCID 11999024 | — |
Reaction Steps
In a microwave reaction tube, 4-chloro-7-azaindole (49, 1.362 g, 8.926 mmol), prepared from 7-azaindole following published procedure (Schneller, S. W.; Luo, Jiann-Kuan. J. Org. Chem. 1980, 45, 4045-4048), 3,4-dimethoxyphenyl boronic acid (4.06 g, 22.3 mmol), and tetrakis(triphenylphosphine)palladium(0) (52 mg, 0.45 mmol) were mixed in 1.0 M potassium carbonate in water (27 mL) and tetrahydrofuran (43 mL). The resulting mixture was heated at 150° C. in a CEM Discover microwave unit for 20 minutes. Ethyl acetate and water were added, and the two layers were separated. The aqueous layer was extracted with ethyl acetate. The combined organic layers were washed with brine and dried over anhydrous sodium sulfate. Concentration under reduced pressure afforded the crude material, which was purified by column chromatography (40-70% ethyl acetate in hexane) to yield the desired product in light yellow solid (50, 974 mg, 3.83 mmol). MS(ESI) [M+H+]+=255.2.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07605168B2 |
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| Source dataset | uspto-grants-2009_10 |
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| ORD ID | ord-315f66e012a74002863f089961bf69cc |
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| Source note | uspto-grants-2009_10 |
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