HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylamine → HCID 59441838, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylamine | HCID 674 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | HCID 59441858 | HCID 59441858 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Tetrahydrofuran | HCID 8028 | — |
| Product | HCID 59441838 | HCID 59441838 | — |
Reaction Steps
A solution of 1-(bromoacetyl)-4,4-dimethyl-6-(methyloxy)-7-nitro-1,2,3,4-tetrahydroquinoline (1.0 g, 2.8 mmol) in tetrahydrofuran (35 mL) was treated with potassium carbonate (1.3 g, 9.4 mmol) and dimethyl amine (10 mL, 20 mmol, 2 M in THF, Aldrich). The mixture was heated in sealed tube at 55° C. for 1h, cooled, diluted with water, and extracted with ethyl acetate. The organic layer was separated, dried over magnesium sulfate, filtered, and concentrated to give {2-[4,4-dimethyl-6-(methyloxy)-7-nitro-3,4-dihydro-1(2H)-quinolinyl]-2-oxoethyl}dimethylamine which was taken directly to the next step. ESIMS (M+H)+=322.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07981903B2 |
| Source dataset | uspto-grants-2011_07 |
| ORD ID | ord-a22d2c0df11c4777b87bb9ac1497df6c |
| Source note | uspto-grants-2011_07 |