HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 967060Generated: October 26, 2026
Methanol → 1-(2-{[3-(3,4-dimethylphenyl)-2-propynyl]oxy}ethyl]-1H-imidazo[4,5-c]quinolin-4-amine
https://huagongshe.com/reaction/967060
Participants
| Role | Name | HCID | Charge |
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| Reactant | Methanol | HCID 887 | — |
| Reactant | Pyrrolidine | HCID 31268 | — |
| Reactant | 4-Iodo-1,2-dimethylbenzene | HCID 141646 | — |
| Reactant | 1-[2-(2-propynyloxy)ethyl)-1H-imidazo[4,5-c]quinolin-4-amine | HCID 9856610 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Catalyst | HCID 178418476 | HCID 178418476 | — |
| Solvent | Chloroform | HCID 6212 | — |
| Product | 1-(2-{[3-(3,4-dimethylphenyl)-2-propynyl]oxy}ethyl]-1H-imidazo[4,5-c]quinolin-4-amine | HCID 22254463 | 14.2% |
Reaction Steps
Under a nitrogen atmosphere, 1-[2-(2-propynyloxy)ethyl]-1H-imidazo[4,5-c]quinolin-4-amine (0.5 g, 1.9 mmol), copper (I) iodide (0.036 g, 0.2 mmol), 4-iodo-ortho-xylene (0.5 g, 2.1 mmol) and pyrrolidine (10 mL) were combined and stirred at ambient temperature. Dichlorobis(triphenylphosphine)palladium(II) (0.066 g, 0.1 mmol) was added and the reaction mixture was stirred at ambient temperature for 1 hour. Analysis by TLC (30% methanol in chloroform) indicated that starting material was still present. The reaction mixture was heated at 65° C. overnight. The pyrrolidine was removed under reduced pressure. The resulting residue was triturated with dichloromethane containing methanol. The insoluble material was isolated by filtration and then recrystallized from toluene (40 mL) to provide 0.1 g of 1-(2-{[3-(3,4-dimethylphenyl)-2-propynyl]oxy}ethyl]-1H-imidazo[4,5-c]quinolin-4-amine as a solid, m.p. 214-216° C. Analysis: Calculated for C23H22N4O: % C, 74.57; % H, 5.99; % N, 15.12. Found: % C, 74.24; % H, 5.98; % N, 15.08.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06953804B2 |
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| Source dataset | uspto-grants-2005_10 |
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| ORD ID | ord-5c33fc56f3fb4035bca18cf49bd36872 |
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| Source note | uspto-grants-2005_10 |
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