Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Sodium Iodide | HCID 5238 | — |
| Reactant | 2-Chloroethyl methyl sulfide | HCID 10965 | — |
| Reactant | Potassium Hydroxide | HCID 14797 | — |
| Reactant | HCID 15501266 | HCID 15501266 | — |
| Solvent | Dimethyl Sulfoxide | HCID 679 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 21712802 | HCID 21712802 | — |
Reaction Steps
Under nitrogen atmosphere, potassium hydroxide (147 mg) in dimethyl sulfoxide (10 ml) was stirred at room temperature for 30 minutes. To the solution were added 2,3-dihydro-6-methoxycarbonyl-2-oxothieno[2,3-b][1,4]thiazine (0.50 g), sodium iodide (0.39 g) and 2-chloroethyl methyl sulfide (0.26 ml), and the mixture was stirred at 50° C. for 6.5 hours. The mixture was poured into water and extracted with ethyl acetate. The organic layer was washed with water and brine, dried over anhydrous sodium sulfate and evaporated under reduced pressure. The residue was purified by column chromatography on silica gel (eluent:hexane:ethyl acetate=3:1) to give 2,3-dihydro-6-methoxycarbonyl-1-[2-(methylthio)-ethyl]-2-oxothieno[2,3-b][1,4]thiazine (465 mg).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06274619B1 |
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| Source dataset | uspto-grants-2001_08 |
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| ORD ID | ord-2374a00467914545a8fbe59ff551aaf4 |
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| Source note | uspto-grants-2001_08 |
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