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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1108648Generated: October 31, 2026

HCID 18783946, compound → HCID 18783941, compound

https://huagongshe.com/reaction/1108648

Reaction equation

Participants

RoleNameHCIDCharge
ReactantHCID 18783946HCID 18783946—
CatalystHCID 178418390HCID 178418390—
SolventMethanolHCID 887—
ProductHCID 18783941HCID 1878394175.4%

Reaction Steps

2.50 g (6.33 mmol) of 4-[4-(tert-Butoxycarbonylamino)butylamino]-2-chloro-3-nitroquinoline was dissolved in 65 ml of methanol and 1 g of 10% palladium-carbon was added thereto. The mixture was stirred for one day under hydrogen atomosphere. The reaction mixture was filtered, the filtrate was concentrated under reduced pressure, and the residue was purified by silica gel column chromatography (chloroform:methanol=10:1 (v/v)). Finally, the resulting product was triturated with diethyl ether and collected by filtration to obtain 1.75 g (4.77 mmol) of 3-amino-4-[4-(tert-butoxycarbonylamino)butylamino]quinoline hydrochloride shown below as a yellow solid. ##STR57## Its spectroscopic data are as follows: IR (KBr) cm-1 : 3340, 2970, 1690, 1590, 1530, 1170.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06069149
Source datasetuspto-grants-2000_05
ORD IDord-82244d514bbf4a1bb2e4af4cd130412c
Source noteuspto-grants-2000_05