HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108638Generated: October 31, 2026
Trifluoroacetic acid → HCID 18783933, compound
https://huagongshe.com/reaction/1108638
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Trifluoroacetic acid | HCID 6422 | — |
| Reactant | HCID 18783939 | HCID 18783939 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 18783933 | HCID 18783933 | 61.4% |
Reaction Steps
0.10 g (0.267 mmol) of 1-[4-(tert-butoxycarbonylamino)butyl]-4-chloro-1H-imidazo-[4,5-c]quinoline was dissolved in 6 ml of methylene chloride. 0.21 ml (2.67 mmol) of trifluoroacetic acid was added thereto and the mixture was concentrated under reduced pressure. 2 ml of a 1N sodium hydroxide aqueous solution and brine were added to the residue and the mixture was extracted five times with chloroform. The extract was dried (Na2SO4) and concentrated under reduced pressure. The residue was triturated with diethyl ether (containing a small amount of methylene chloride) and the precipitate thus formed was collected by filtration to obtain 45 mg (0.164 mmol) of 1-(4-aminobutyl)-4-chloro-1H-imidazo[4,5-c]quinoline (shown below) as pale orange powder. ##STR44## Its spectroscopic data are as follows: IR (KBr) cm-1 : 3400, 2950, 1670, 1520, 1360.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06069149 |
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| Source dataset | uspto-grants-2000_05 |
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| ORD ID | ord-47a0af90b87f412d91d555edb98bdd6c |
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| Source note | uspto-grants-2000_05 |
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