HuagongsheHuagongshe Chemistry Print Report · For research reference only
Dimethylformamide → 6-Isobutoxy-2-(2-pyridyl)-4H-1,3-benzothiazine-4-one
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | Dimethylformamide | HCID 6228 | — |
| Reactant | 1-Bromo-2-methylpropane | HCID 6555 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | 6-hydroxy-2-(2-pyridyl)-4H-1,3-benzothiazine-4-one | HCID 22939470 | — |
| Solvent | Water | HCID 962 | — |
| Product | 6-Isobutoxy-2-(2-pyridyl)-4H-1,3-benzothiazine-4-one | HCID 59750181 | 19.7% |
Reaction Steps
A mixture of 6-hydroxy-2-(2-pyridyl)-4H-1,3-benzothiazine-4-one (0.35 g, 1.3 mmol), isobutyl bromide (0.64 g, 4.6 mmol) and potassium carbonate (0.57 g, 4.1 mmol) and DMF (10 ml) was stirred at room temperature for 15 hrs. The reaction mixture was diluted with water and extracted with ethyl acetate. The extract was washed with water and dried. The solvent was evaporated. The residue was subjected to a silica gel column chromatography and eluted with hexane-ethyl acetate (2:1, v/v). The obtained crystals were recrystallized from ethyl acetate-hexane to give the titled compound (0.08 g, 19%).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US07399759B2 |
| Source dataset | uspto-grants-2008_07 |
| ORD ID | ord-0a0504809583491cae3320e8ff457de0 |
| Source note | uspto-grants-2008_07 |