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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108639Generated: October 28, 2026

Benzylamine → HCID 18783936, compound

https://huagongshe.com/reaction/1108639

Reaction equation

Participants

RoleNameHCIDCharge
ReactantBenzylamineHCID 7504—
ReactantHCID 18783939HCID 18783939—
ProductHCID 18783936HCID 18783936—

Reaction Conditions

Temperature150 °C

Reaction Steps

2 ml of benzylamine was added to 70 mg (0.187 mmol) of 1-[4-(tert-butoxycarbonylamino)butyl]-4-chloro-1H-imidazo-[4,5-c]quinoline. The resulting mixture was heated at 150° C. and stirred for 3 hours. An excess amount of benzylamine was distilled off under reduced pressure and 1N hydrochloric acid and brine were added thereto. The resulting solution was extracted twice with methylene chloride. The organic phase was washed with a saturated sodium hydrogencarbonate aqueous solution and dried (Na2SO4). The solvent was then distilled off under reduced pressure. The residue was purified by silica gel column chromatography (chloroform:methanol=150:1 (v/v)) to obtain 79 mg (0.177 mmol) of 4-benzylamino-1-[4-(tert-butoxycarbonylamino)butyl]-1H-imidazo[4,5-c]quinoline shown below as white powder (mp: 151 to 153.5° C.). ##STR46## Its spectroscopic data are as follows: IR (KBr) cm-1 : 3380, 3310, 2930, 1680, 1595, 1540, 1245, 1160.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069149
Source datasetuspto-grants-2000_05
ORD IDord-8531154080ab49deb39533ee170dc0be
Source noteuspto-grants-2000_05