HuagongsheHuagongshe Chemistry Print Report · For research reference only
Water → HCID 23022717, compound
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 2-Butanone, 3-bromo- | HCID 13142 | — |
| Reactant | HCID 85824834 | HCID 85824834 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Solvent | Ethyl Acetate | HCID 8857 | — |
| Product | HCID 23022717 | HCID 23022717 | 73.3% |
Reaction Steps
N-{4-[(6,7-Dimethoxy-4-quinolyl)oxy]phenyl}thiourea (50 mg) was dissolved in dimethylformamide (5 ml) to prepare a solution. Triethylamine (43 mg) and 3-bromo-2-butanone (43 mg) were added to the solution, and the mixture was stirred at room temperature for 3 hr. Water and ethyl acetate were added to the reaction solution, and the mixture was extracted with ethyl acetate. The extract was then washed with saturated brine and was dried over anhydrous sodium sulfate, and the solvent was removed by evaporation under the reduced pressure. The crude thus obtained was purified by column chromatography on silica gel using chloroform/methanol for development to give the title compound (42 mg, yield 73%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07495104B2 |
| Source dataset | uspto-grants-2009_02 |
| ORD ID | ord-d93b8e625e66444fb17b851abd439eee |
| Source note | uspto-grants-2009_02 |