참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Selenium Dioxide | HCID 24007 | — |
| 반응물 | 1,2-Dimethyl-1H-imidazo[4,5-c]pyridine | HCID 4287394 | — |
| 용매 | 1,4-Dioxane | HCID 31275 | — |
| 생성물 | 1-Methyl-1H-imidazo(4,5-c)pyridine-2-carboxaldehyde | HCID 12239331 | 73% |
반응 단계
To a solution of 1,2-dimethyl-1H-imidazo[4,5-c]pyridine (500 mg, 3.40 mmol) in dry 1,4-dioxane (7.5 mL) was added http://newsearchch.chemexper.com/cheminfo/servlet/org.dbcreator.MainServlet?sort=%3E%7Eentry.int Value&query=structure._structureID%3D4635571 &target=entry&action=PowerSearch&onclick=1 &from=0 &history=off&forGroupNames=&style=&realQuery=rn.value%3D%22CF3 COOH%22+elsor+entry.catalogID%3D%22CF3 COOH%22+elsor+iupac.value%3D%22CF3 COOH%22+elsor+mf.value%3D%22CF3 COOH%22+elsor+%28iupac.value%3D%7E%22CF3 COOH%22+ or +catalog.description%3D%7E%22CF3 COOH%22%29&format=ccd&searchTemplate=rn.value%3D%3F+elsor+entry.catalogID%3D%3 selenium dioxide (665 mg, 5.10 mmol). The mixture heated by microwave at 130° C. for 5 min. Then the mixture was filtered and concentrated to give the crude product, which was purified by column chromatography (silica gel, petroleum ether:DCM 10:1 to 1:1) to give the title compound (400 mg, yield 28%). LC-MS (ESI) m/z: 162 (M+1)+. 1H-NMR (400 MHz, CD3OD) δ (ppm): 3.61 (s, 3H), 5.91 (s, 1H), 7.67-7.70 (d, J=5.6 Hz, 1H), 8.39-8.41 (d, J=5.6 Hz, 1H), 8.93 (s, 1H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|
| 특허 번호 | US08420650B2 |
|---|
| 출처 데이터셋 | uspto-grants-2013_04 |
|---|
| ORD ID | ord-20b4d9807cc84e2ea17adc5587d13356 |
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| 출처 메모 | uspto-grants-2013_04 |
|---|