HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1058631Generated: November 2, 2026
Hydrochloric Acid → 4-Amino-1-[2-(4-piperidyl)ethyl]-1h-imidazo[4,5-c]quinoline hydrochloride
https://huagongshe.com/reaction/1058631
Participants
| Role | Name | HCID | Charge |
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| Reactant | Hydrochloric Acid | HCID 313 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium Hydroxide | HCID 14798 | — |
| Reactant | HCID 18668744 | HCID 18668744 | — |
| Solvent | Water | HCID 962 | — |
| Product | 4-Amino-1-[2-(4-piperidyl)ethyl]-1h-imidazo[4,5-c]quinoline hydrochloride | HCID 18668799 | — |
Reaction Steps
A mixture of 1.57 g of tert-butyl 4-[2-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)ethyl]-1-piperidinecarboxylate and 40 ml of ethyl acetate solution of hydrogen chloride was stirred at room temperature for 5 hours. The reaction mixture was added with water, adjusted to pH 10 with 10% aqueous sodium hydroxide solution, and extracted with methylene chloride. The extract was dried, and the solvent was evaporated. The resulting residue was washed with ethyl acetate to give 1.01 g of pale brown crystals. The resulting crystals were purified by alumina column chromatography using methylene chloride—methanol (40:1 to 20:1) as eluting solvents, and washed with diisopropyl ether to give colorless crystals. Hydrochloride was prepared in a conventional method. Recrystallization from ethanol gave colorless crystals having the melting point of from 243 to 244° C. (decomposition).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06518265B1 |
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| Source dataset | uspto-grants-2003_02 |
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| ORD ID | ord-a1698816b7824719b956d51eafa72079 |
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| Source note | uspto-grants-2003_02 |
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