Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Water | HCID 962 | — |
| Reactant | Ethyl Acetate | HCID 8857 | — |
| Reactant | Sodium methanethiolate | HCID 4378561 | — |
| Reactant | 6-(4-oxo-4H-1,3-benzothiazin-2-yl)-2-pyridylmethanesulfonate | HCID 86596462 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | HCID 22939303 | HCID 22939303 | 75% |
Reaction Steps
[6-(4-Oxo-4H-1,3-benzothiazin-2-yl)-2-pyridyl]methanesulfonate (0.55 g, 1.58 mmol) was dissolved in DMF (30 ml), and sodium thiomethoxide (0.13 g, 1.74 mmol) was added thereto. The mixture was stirred at 70° C. for 3 hrs. The reaction mixture was combined with ethyl acetate and water. The organic layer was washed with saturated brine and dried over anhydrous magnesium sulfate. The solvent was evaporated. The residue was recrystallized from ethanol to give the titled compound (0.35 g, 75%) as pale yellow crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07399759B2 |
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| Source dataset | uspto-grants-2008_07 |
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| ORD ID | ord-08c2559a54b24541ae444743e5af66ac |
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| Source note | uspto-grants-2008_07 |
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