Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Morpholine | HCID 8083 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | N,N-Dimethylglycine hydrochloride | HCID 75605 | — |
| Reactant | HCID 67440706 | HCID 67440706 | — |
| Catalyst | Copper(1+) iodide; Copper(I) iodide; Cuprous iodide; Cuprous iodide (CuI) | HCID 24350 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 67441721 | HCID 67441721 | 36% |
Reaction Steps
A mixture of 2-(3-bromo-5-methoxy-phenyl)-3,3-dimethyl-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.85 g, 2.0 mmol), morpholine (1.77 g, 20 mmol), copper (I) iodide (0.23 g, 1.2 mmol), N,N-dimethylglycine hydrochloride (0.22 g, 1.6 mmol) and potassium carbonate (0.83 g, 6.0 mmol) in DMSO (5 mL) was heated for 4 hours at 120° C. After cooling to room temperature, the mixture was treated with ethyl acetate (50 mL) and washed with water (20 mL). The organic layer was dried over anhydrous sodium sulfate and concentrated in vacuo. Purification on flash silica gel chromatography (silica gel from QingDao, 200-300 mesh, glass column from Shanghai SD company)(20% ethyl acetate/hexanes) to afford 3,3-dimethyl-2-(3-methoxy-5-morpholin-4-yl-phenyl)-1,2,3,4-tetrahydro-quinoline-6-carboxylic acid ethyl ester (0.30 g, 36%) as a white solid: LC/MS m/e calcd for C25H32N2O4 (M+H)+: 425.5, observed: 425.3.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08586747B2 |
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| Source dataset | uspto-grants-2013_11 |
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| ORD ID | ord-b199db8164524a2d96143e26587da300 |
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| Source note | uspto-grants-2013_11 |
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