HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 649152Generated: October 29, 2026
Ethanol → 7-Chloro-3-(1-imidazolylmethyl)-2-methylimidazo[2,1-a]isoquinoline
https://huagongshe.com/reaction/649152
Participants
| Role | Name | HCID | Charge |
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| Reactant | Ethanol | HCID 702 | — |
| Reactant | Imidazole | HCID 795 | — |
| Reactant | 7-Chloro-2-methyl-3-trimethylammoniomethylimidazo[2,1-a]isoquinoline methylsulfate | HCID 13821864 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | 7-Chloro-3-(1-imidazolylmethyl)-2-methylimidazo[2,1-a]isoquinoline | HCID 70419806 | 41% |
Reaction Steps
Ethanol (50 ml) was added to a mixture of 7-chloro-2-methyl-3-trimethylammoniomethylimidazo[2,1-a]isoquinoline methylsulfate (2.3 g) and imidazole (0.95 g) in dimethyl sulfoxide (20 ml) and heated at 100° C. with stirring for 5 hours. After the removal of ethanol by distillation, the residue was poured into water. The resulting precipitates were collected by filtration, dried and recrystallized from ethyl acetate. The obtained crystals were chromatographed on silica gel (16 g) with a mixture of chloroform and methanol (10:1) as an eluent. The eluates were evaporated in vacuo and the residual solid was recrystallized from ethyl acetate to give 7-chloro-3-(1-imidazolylmethyl)-2-methylimidazo[2,1-a]isoquinoline (0.7 g).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US04738967 |
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| Source dataset | uspto-grants-1988_04 |
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| ORD ID | ord-d3fcd37c1fb04a1a9f81100b2f53b7e0 |
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| Source note | uspto-grants-1988_04 |
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