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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2182286Generated: October 31, 2026

4-Morpholinecarbonyl chloride → HCID 9820621, compound

https://huagongshe.com/reaction/2182286

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]-4-morpholinecarboxamide as a tan powder, m.p. 177.0-179.5° C. 1H NMR (300 MHz, DMSO-d6) δ 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 numberUS06897221B2
Source datasetuspto-grants-2005_05
ORD IDord-ec6369fa426844aa982a39effa012f11
Source noteuspto-grants-2005_05