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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2047697Generated: October 30, 2026

Morpholine → HCID 66587793, compound

https://huagongshe.com/reaction/2047697

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMorpholineHCID 8083—
ReactantL-ProlineHCID 145742—
ReactantHCID 66587676HCID 66587676—
CatalystCopper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI)HCID 24350—
SolventDimethyl SulfoxideHCID 679—
SolventWaterHCID 962—
ProductHCID 66587793HCID 6658779352.6%

Reaction Conditions

Temperature120 °C

Reaction Steps

The mixture of 4,4-dimethyl-2-(3-bromo-phenyl)-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid methyl ester as prepared according to Example 1 (374 mg, 1 mmol), CuI (60 mg, 0.3 mmol), L-proline (70 mg, 0.6 mmol) and morpholine (440 mg, 5 mmol) in DMSO (5 mL) was stirred at 120° C. for 16 hours under a nitrogen atmosphere. The reaction mixture was diluted with water (20 mL), extracted with ethyl acetate (20 mL×3) and washed with brine (100 mL) and then dried over anhydrous Na2SO4. The solvent was removed in vacuo and the residue was purified by ISCO combi-flash chromatography (gradient elution, 30-60% ethyl acetate in petroleum ether) to afford 4,4-dimethyl-2-(3-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid methyl ester (200 mg, 52.6%) as a white solid. MS (ESI+) [(M+H)+] 381.1.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS08592594B2
Source datasetuspto-grants-2013_11
ORD IDord-1f9b8125dcf547ceabfacb1eb6c80b54
Source noteuspto-grants-2013_11