HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → 2-((Cyclobutylmethyl)(ethyl)amino)-8-methylquinoline-3-carbaldehyde
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 2-Chloro-8-methylquinoline-3-carboxaldehyde | HCID 689082 | — |
| Reactant | (Cyclobutylmethyl)(ethyl)amine | HCID 23366322 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | 2-((Cyclobutylmethyl)(ethyl)amino)-8-methylquinoline-3-carbaldehyde | HCID 57486842 | 75% |
Reaction Steps
Potassium carbonate (0.62 g, 4.5 mmol) was added to a solution of 2-chloro-8-methyl-quinoline-3-carbaldehyde (0.45 g, 2.2 mmol) and cyclobutylmethyl-ethyl-amine (0.47 g, 4.1 mmol) in anhydrous dimethyl formamide (5 mL) under nitrogen. After stirring for 0.5 h at RT, the reaction mixture was heated for 20 h at 80-95° C. Thereafter, the reaction was cooled to RT, water (30 mL) and ethyl acetate (30 mL) were added, and the organic layer was separated from the aqueous mixture. The organic extract was washed with brine, dried over sodium sulfate and the solvent was evaporated in vacuo. The residue was purified by chromatography using silica gel to afford the title compound as a pale yellow liquid (0.46 g, 75%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08604055B2 |
| Source dataset | uspto-grants-2013_12 |
| ORD ID | ord-bdfbe09040d94836af576c32d8a12371 |
| Source note | uspto-grants-2013_12 |