HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 966046Generated: October 30, 2026
1,2-Dimethoxyethane → 1-(1-Ethylpropyl)-6-mesityl-4-methyl-2,3-dihydro-1H-pyrrolo[3,2-c]quinoline
https://huagongshe.com/reaction/966046
Participants
| Role | Name | HCID | Charge |
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| Reactant | 1,2-Dimethoxyethane | HCID 8071 | — |
| Reactant | Barium hydroxide, octahydrate | HCID 17749109 | — |
| Reactant | Mesitylboric acid | HCID 22237855 | — |
| Reactant | 1-(1-Ethylpropyl)-6-iodo-4-methyl-2,3-dihydro-1H-pyrrolo[3,2-c]quinoline | HCID 22249956 | — |
| Catalyst | HCID 178418397 | HCID 178418397 | — |
| Solvent | Water | HCID 962 | — |
| Product | 1-(1-Ethylpropyl)-6-mesityl-4-methyl-2,3-dihydro-1H-pyrrolo[3,2-c]quinoline | HCID 22249759 | 15.2% |
Reaction Steps
1-(1-Ethylpropyl)-6-iodo-4-methyl-2,3-dihydro-1H-pyrrolo[3,2-c]quinoline (200 mg, 0.526 mmol), mesitylboric acid (95 mg, 0.579 mmol), barium hydroxide octahydrate (249 mg, 0.782 mmol) and tetrakistriphenylphosphinepalladium (12 mg, 0.01 mmol) were suspended into a mixture of dimethoxyethane (6 mL) and water (1 mL), followed by stirring at 80° C. for two days in nitrogen atmosphere. Water was added to the reaction mixture, followed by extracting with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous magnesium sulfate, and then evaporated. The residue was purified by silica gel column chromatography (ethyl acetate), to give the title compound (28 mg, 0.08 mmol) as a pale yellow oil.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06951865B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-02637e7d687e415ea36929676a33a8b5 |
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| Source note | uspto-grants-2005_10 |
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