HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → Ethyl 7-((dimethylamino)thioxomethoxy)-4-oxo-8-propyl-4H-1-benzopyran-2-carboxylate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | Sodium hydride | HCID 24758 | — |
| Reactant | Ethyl 7-hydroxy-4-oxo-8-propyl-4H-chromene-2-carboxylate | HCID 4196515 | — |
| Reactant | Dimethylaminothiocarbamylchloride | HCID 14673822 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | Ethyl 7-((dimethylamino)thioxomethoxy)-4-oxo-8-propyl-4H-1-benzopyran-2-carboxylate | HCID 13744907 | — |
Reaction Steps
Ethyl 7-hydroxy-4-oxo-8-n-propyl-4H-1-benzopyran-2-carboxylate (1 g) in anhydrous dimethylformamide (4 ml) is cooled to 0° and treated under nitrogen with sodium hydride (50% dispersion in mineral oil, 180 mg) with stirring for 30 minutes. Dimethylaminothiocarbamylchloride (465 mg) is added and the mixture is stirred 15 minutes at 0°, warmed to 80° and maintained as such for 18 hours. The mixture is cooled, diluted with methylene chloride (50 ml) and washed with water (3×100 ml)), dried over sodium sulfate and reduced to dryness in vacuo. The residue is recrystallized from ethyl acetate and hexane to yield the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05314918 |
| Source dataset | uspto-grants-1994_05 |
| ORD ID | ord-b34ba0936ec743b8aba301b1a89049fe |
| Source note | uspto-grants-1994_05 |