HuagongsheHuagongshe Chemistry Print Report · For research reference only
Iodoethane → 2-Ethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Iodoethane | HCID 6340 | — |
| Reactant | 4-Hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide | HCID 54690657 | — |
| Solvent | Methanol | HCID 887 | — |
| Solvent | Sodium Hydroxide | HCID 14798 | — |
| Product | 2-Ethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide | HCID 54690138 | 48% |
Reaction Steps
0.94 gm (6 millimols) of ethyl iodide were added to a solution of 0.7 gm (2 millimols) of 4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide in 30 ml of methanol and 2.0 ml of 1N sodium hydroxide. The reaction mixture was stirred for 24 hours at room temperature, then neutralized and evaporated in vacuo. The residue was purified by column chromatography (Merck-silica gel 60, particle size: 0.2-0.5 mm; eluant: chloroform/ethanol 95:5), yielding 0.35 mgm (48% of theory) of 2-ethyl-4-hydroxy-N-(5-methyl-2-thiazolyl)-2H-1,2-benzothiazine-3-carboxamide-1,1-dioxide after recrystallization from xylene.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US04233299 |
| Source dataset | uspto-grants-1980_11 |
| ORD ID | ord-7e8dbc42e9ab41089cf19bcbf3bdcc76 |
| Source note | uspto-grants-1980_11 |