HuagongsheHuagongshe Chemistry Print Report · For research reference only
2-Thiophenecarboxaldehyde → 5-(Benzoxazol-2-yl)-2-(thiophen-2-yl)-1-(tetrahydropyran-4-yl)benzimidazole
Participants
| Role | Name | HCID | Charge |
|---|---|---|---|
| Reactant | 2-Thiophenecarboxaldehyde | HCID 7364 | — |
| Reactant | Potassium Carbonate | HCID 11430 | — |
| Reactant | Potassium hydroxy sulfite | HCID 23707502 | — |
| Reactant | 5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline | HCID 67498806 | — |
| Solvent | Water | HCID 962 | — |
| Solvent | Dimethylformamide | HCID 6228 | — |
| Product | 5-(Benzoxazol-2-yl)-2-(thiophen-2-yl)-1-(tetrahydropyran-4-yl)benzimidazole | HCID 67498280 | 36% |
Reaction Steps
5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (0.13 g, 0.42 mmol) was dissolved in DMF (3 mL) and water (0.1 mL), 2-thiophenecarbaldehyde (0.05 g, 0.45 mmol) was added followed by oxone (0.17 g, 0.28 mmol), and this was stirred at room temperature for 2.5 hours. Aqueous potassium carbonate solution (0.10 g/15 mL) was added to the reaction solution. This was extracted with ethyl acetate, washed with water, and after drying over magnesium sulfate, this was concentrated and purified by silica gel column chromatography. The crystals obtained were washed with hexane and a small amount of ethyl acetate, and dried to yield the title compound (60 mg, 36% yield) as light brown crystals.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patent number | US08829035B2 |
| Source dataset | uspto-grants-2014_09 |
| ORD ID | ord-a987402ca7234d9289113b220d456175 |
| Source note | uspto-grants-2014_09 |