HuagongsheHuagongshe Chemistry Print Report · For research reference only
Potassium Iodide → Ethyl 2-[4-(5-chlorobenzothiazol-2-yl) methyl-3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl]acetate
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Potassium Iodide | HCID 4875 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Ammonium Chloride | HCID 25517 | — |
| Reactant | Ethyl (3-oxo-3,4-dihydro-2h-1,4-benzoxazine-2-yl)acetate | HCID 15292312 | — |
| Reactant | 2-(Bromomethyl)-5-chloro-1,3-benzothiazole | HCID 15292313 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Product | Ethyl 2-[4-(5-chlorobenzothiazol-2-yl) methyl-3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl]acetate | HCID 15292314 | — |
Reaction Steps
Ethyl 2-(3,4-dihydro-3-oxo-2H-1,4-benzoxazin-2-yl]acetate (150 mg), 2-bromomethyl-5-chlorobenzothiazole (186 mg) and potassium iodide (13 mg) were dissolved in dimethyl sulfoxide (2 ml). Potassium carbonate (133 mg) was added and the mixture was stirred at room temperature for 15 hours. A saturated aqueous solution of ammonium chloride was added to the reaction mixture, and the mixture was extracted with ethyl acetate. The organic layer was washed with saturated brine and dried over anhydrous sodium sulfate, and the solvent was distilled away.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US05635505 |
| Source dataset | uspto-grants-1997_06 |
| ORD ID | ord-3bee6e69b6374e498dbfb46ae3ead3c6 |
| Source note | uspto-grants-1997_06 |