참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Water | HCID 962 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | 5-Chloroimidazo[1,2-A]pyridine | HCID 10953722 | — |
| 반응물 | (4-Hydroxypiperidin-1-yl)(thiophen-2-yl)methanone | HCID 23362856 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 5-[1-(2-Thienylcarbonyl)-4-piperidyloxy]imidazo[1,2-a]pyridine | HCID 23362964 | 4.6% |
반응 단계
To a suspension of 60% sodium hydride in oil (0.40 g, 10 mmoles) in dimethylformamide (30 ml) was added 1-(2-thienylcarbonyl)-4-hydroxypiperidine (2.11 g, 10 mmoles) with stirring under ice-cooling and the mixture was stirred at room temperature for 30 minutes. To this reaction mixture was added 5-chloroimidazo[1,2-a]pyridine (1.53 g, 10 mmoles) with stirring under ice-cooling, followed by stirring at room temperature for 7 hours. Water was added to the reaction mixture, which was extratced with ethyl acetate and dried. After the solvent was distilled off, the residue was purified with column chromatography [eluent: ethyl acetate/hexane (1:1)→ethyl acetate/hexane (2:1)→ethyl acetate/ethanol (50:1)] to obtain 0.15 g of the desired product (4.6%, pale yellow oily product).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US05395839 |
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| 출처 데이터셋 | uspto-grants-1995_03 |
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| ORD ID | ord-f920119d838e4b049080b711ad6eda16 |
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| 출처 메모 | uspto-grants-1995_03 |
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