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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108634Generated: October 30, 2026

4-benzylamino-1-[3-(tert-butoxycarbonylamino)propyl]-1H-imidazo[4,5-c]quinoline → 1-(3-aminopropyl)-1H-imidazo[4,5-c]quinoline-4-amine

https://huagongshe.com/reaction/1108634

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-benzylamino-1-[3-(tert-butoxycarbonylamino)propyl]-1H-imidazo[4,5-c]quinolineHCID 18783952—
CatalystHCID 178502593HCID 178502593—
SolventFormic AcidHCID 284—
Product1-(3-aminopropyl)-1H-imidazo[4,5-c]quinoline-4-amineHCID 1878397341.7%

Reaction Steps

30 mg (0.0695 mmol) of 4-benzylamino-1-[3-(tert-butoxycarbonylamino)propyl]-1H-imidazo[4,5-c]quinoline was dissolved in 3 ml of formic acid. 0.1 g of 20% palladium hydroxide-carbon was added thereto and the mixture was refluxed under heating for one day. The reaction mixture was filtered and the filtrate was evaporated to distill off the solvent under reduced pressure. The resulting residue was purified by silica gel column chromatography (chloroform: methanol:32% acetic acid=6:3:1 (v/v)) to obtain the acetic acid salt of the object. The thus obtained product was subjected to treatment with alkali to obtain the free base. The precipitate thus formed was collected by filtration to obtain 7 mg (0.0290 mmol) of 1-(3-aminopropyl)-1H-imidazo[4,5-c]quinoline-4-amine shown below as faint brown powder. ##STR40## The physicochemical data of this compound was in agreement with compound of Example 5.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069149
Source datasetuspto-grants-2000_05
ORD IDord-385ecafbf5eb495f8f66c7306af9c2dd
Source noteuspto-grants-2000_05