Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
3-Pyridinecarboxaldehyde → 5-(Benzoxazol-2-yl)-2-(3-pyridyl)-1-(tetrahydropyran-4-yl)benzimidazole
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | 3-Pyridinecarboxaldehyde | HCID 10371 | — |
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | Potassium hydroxy sulfite | HCID 23707502 | — |
| 반응물 | 5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline | HCID 67498806 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 5-(Benzoxazol-2-yl)-2-(3-pyridyl)-1-(tetrahydropyran-4-yl)benzimidazole | HCID 67497893 | 49.5% |
반응 단계
5-(Benzoxazol-2-yl)-2-(tetrahydropyran-4-yl)aminoaniline (see Working Example 20-2) (0.15 g, 0.484 mmol) was dissolved in DMF (3 mL) and water (0.1 mL), 3-pyridinecarboxaldehyde (0.06 g, 0.561 mmol) was added followed by oxone (0.19 g, 0.310 mmol), and this was stirred at room temperature for 2.5 hours. Aqueous potassium carbonate solution (0.09 g/15 mL) was added to the reaction solution. This was extracted with chloroform, 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 (95.0 mg, 49.5% yield) as white crystals.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US08829035B2 |
| 출처 데이터셋 | uspto-grants-2014_09 |
| ORD ID | ord-897d73089fb64b02b603065e4363a006 |
| 출처 메모 | uspto-grants-2014_09 |