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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 82008Generated: October 29, 2026

Morpholine → HCID 66571344, compound

https://huagongshe.com/reaction/82008

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantPhosphorus oxychlorideHCID 24813—
Reactant7-(3,5-Dimethyl-4-isoxazolyl)-8-(methyloxy)-1-[(1R)-1-phenylethyl]-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-oneHCID 52935183—
SolventDimethyl SulfoxideHCID 679—
SolventN-methyl-2-pyrrolidoneHCID 13387—
ProductHCID 66571344HCID 665713440.75%

Reaction Conditions

Temperature100 °C

Reaction Steps

7-(3,5-Dimethyl-4-isoxazolyl)-8-(methyloxy)-1-[(1R)-1-phenylethyl]-1,3-dihydro-2H-imidazo[4,5-c]quinolin-2-one (for a preparation see Intermediate 11) (0.16 g, 0.386 mmol) was dissolved in POCl3 (1 ml, 10.73 mmol) and heated at 100° C. for 3 days. The reaction mixture was evaporated in vacuo to give a black gum. The residue was dissolved in NMP (2 ml) and morpholine (2 ml, 22.96 mmol) was added, then the solution was heated in the microwave at 150° C. for 1 h. The reaction mixture was loaded onto a 20 g SCX-2 cartridge and washed through with methanol (40 ml), then eluted with 2M methanolic ammonia and the eluant evaporated in vacuo to give an amber oil. This was dissolved in DMSO (1 ml) and purified by MDAP (HpH) to give 7-(3,5-dimethyl-4-isoxazolyl)-8-(methyloxy)-2-(4-morpholinyl)-1-[(1R)-1-phenylethyl]-1H-imidazo[4,5-c]quinoline (1.4 mg, 2.90 μmol, 0.750% yield). LCMS (formate) Rt 0.86 min, MH+ 484

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08846709B2
Source datasetuspto-grants-2014_09
ORD IDord-f52e2b1e01ab4a919fbdee63e3d1f7ab
Source noteuspto-grants-2014_09