Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
Nitric Acid → N-(4-((2R,5S)-1-acetyl-5-methylpyrrolidin-2-yl)-5-fluoro-2-nitrophenyl)pyrazine-2-carboxamide
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|---|---|---|
| 반응물 | Nitric Acid | HCID 944 | — |
| 반응물 | N-(4-((5S)-1-acetyl-5-methylpyrrolidin-2-yl)-3-fluorophenyl)pyrazine-2-carboxamide | HCID 67482899 | — |
| 용매 | Chloroform | HCID 6212 | — |
| 생성물 | N-(4-((2R,5S)-1-acetyl-5-methylpyrrolidin-2-yl)-5-fluoro-2-nitrophenyl)pyrazine-2-carboxamide | HCID 67482980 | — |
반응 단계
1 ml of fuming nitric acid was added to 59 mg of N-(4-((5S)-1-acetyl-5-methylpyrrolidin-2-yl)-3-fluorophenyl)pyrazine-2-carboxamide at room temperature, and the reaction liquid was stirred at the same temperature for 30 minutes. The reaction liquid was diluted with chloroform, washed with aqueous saturated sodium bicarbonate, and dried with anhydrous magnesium sulfate. The solvent was evaporated away under reduce pressure, and purified through partitioning thin-layer chromatography (Kieselgel™ 60F254, Art 5744 (by Merck), ethyl acetate) to obtain the entitled compound as a pale yellow oily substance. (Rf: trans form>cis form.)
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| 특허 번호 | US07728025B2 |
| 출처 데이터셋 | uspto-grants-2010_06 |
| ORD ID | ord-b1646f6a829743f383e61eefbf09f40b |
| 출처 메모 | uspto-grants-2010_06 |