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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108638Generated: October 31, 2026

Trifluoroacetic acid → HCID 18783933, compound

https://huagongshe.com/reaction/1108638

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTrifluoroacetic acidHCID 6422—
ReactantHCID 18783939HCID 18783939—
SolventDichloromethaneHCID 6344—
ProductHCID 18783933HCID 1878393361.4%

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

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069149
Source datasetuspto-grants-2000_05
ORD IDord-47a0af90b87f412d91d555edb98bdd6c
Source noteuspto-grants-2000_05