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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1837560Generated: October 31, 2026

4-Morpholinecarbonyl chloride → HCID 9820621, compound

https://huagongshe.com/reaction/1837560

Reaction equation

Participants

RoleNameHCIDCharge
Reactant4-Morpholinecarbonyl chlorideHCID 84810—
Reactant1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amineHCID 15453775—
SolventPyridineHCID 1049—
ProductHCID 9820621HCID 9820621194.5%

Reaction Steps

4-Morpholinecarbonyl chloride (0.15 ml, 1.3 mmol) was added to a stirring solution of 1-(4-aminobutyl)-1H-imidazo[4,5-c]quinolin-4-amine (0.3 g, 1.2 mmol) and pyridine (70 ml). The reaction was maintained at room temperature overnight. The solvent was removed in vacuo and the residue was purified by flash column chromatography (silica gel, 9:1 dichloromethane\methanol). The fractions containing product were combined, washed with saturated aqueous sodium bicarbonate, dried (MgSO4), filtered, and concentrated to provide 0.86 g of N4-[4-(4-amino-1H-imidazo[4,5-c]quinolin-1-yl)butyl]morpholinecarboxamide as a tan powder, m.p. 177.0-179.5° C. 1H NMR (300 MHz, DMSO-d6) δ 5 8.22 (s, 1H), 8.04 (d, J=7.1 Hz, 1H), 7.64 (d, J=7.5 Hz, 1H), 7.47 (t, J=7.1 Hz, 1H), 7.28 (t, J=7.1 Hz, 1H), 6.72 (broad s, 2H), 6.52 (t, J=5.4 Hz, 1H), 4.61 (t, J=6.9 Hz, 2H), 3.48 (t J=4.6 Hz, 4H), 3.18 (t, J=4.6 Hz, 4H), 3.05 (m, 2H), 1.84 (m, 2H), 1.44 (m, 2H); MS (EI) m/e 368.1966 (368.1961 calcd for C19H24N6O2).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06784188B2
Source datasetuspto-grants-2004_08
ORD IDord-5d20e73577cb4e58a4f99b981d49c6ed
Source noteuspto-grants-2004_08