HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1458916Generated: October 27, 2026
Ethyl 2-iodomethyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)quinoline-3-carboxylate → Ethyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-[(1-methyl-2-imidazolyl)oxymethyl]quinoline-3-carboxylate
https://huagongshe.com/reaction/1458916
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethyl 2-iodomethyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)quinoline-3-carboxylate | HCID 21851133 | — |
| Reactant | HCID 178480601 | HCID 178480601 | — |
| Catalyst | Silver carbonate | HCID 92796 | — |
| Solvent | Benzene | HCID 241 | — |
| Product | Ethyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-[(1-methyl-2-imidazolyl)oxymethyl]quinoline-3-carboxylate | HCID 21851189 | 9.4% |
Reaction Steps
A mixture of ethyl 2-iodomethyl-6,7-dimethoxy-4-(3,4-dimethoxyphenyl)quinoline-3-carboxylate (9.0 g), 2-hydroxy-1-methylimidazole (1.8 g), silver (I) carbonate (Ag2CO3)(5.1 g) and benzene (100 ml) was stirred at 50° C. for 18 hours. The insoluble solid was filtered off. The filtrate was washed with water and dried over magnesium sulfate, and the solvent was evaporated. The residual oil was subjected to column chromatography on silica gel. The fractions eluted with chloroform/ethyl acetate (5/1, v/v) gave ethyl 6,7-dimethoxy-4-(3,4-dimethoxyphenyl)-2-[(1-methyl-2-imidazolyl)oxymethyl]quinoline-3-carboxylate (0.8 g, 9%) which was then recrystallized from ethyl acetate-hexane.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US05852039 |
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| Source dataset | uspto-grants-1998_12 |
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| ORD ID | ord-62ea964fcb9a4560b5e0e68e8e718b23 |
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| Source note | uspto-grants-1998_12 |
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