참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 3-Morpholinophenol | HCID 141343 | — |
| 반응물 | Sodium bis(trimethylsilyl)amide | HCID 2724254 | — |
| 반응물 | 3-Fluoro-2-nitropyridine | HCID 2762802 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | 4-(3-(2-Nitropyridin-3-yloxy)phenyl)morpholine | HCID 66995169 | 73.1% |
반응 단계
In a 125 mL round-bottom flask, 3-morpholinophenol (0.91 g, 5.07 mmol) was dissolved in THF (40 mL). Solution was cooled to 0° C. and NaHMDS (5.07 mL, 5.07 mmol) (1M in THF) was added slowly. The mixture was agitated for 15 minutes and solution of 3-fluoro-2-nitropyridine (0.60 g, 4.22 mmol) in THF (5 mL) was added slowly. After agitating for 2 hours the solvent was evaporated and the residue dissolved in 100 mL of CH2Cl2 and washed with diluted sodium bicarbonate solution twice, dried over magnesium sulfate, filtered and evaporated. Crude material was purified by chromatography on silica gel, eluted with 25% ethyl acetate/Hexane to give the title compound (0.93 g, 72%) was obtained as thick red oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08883828B2 |
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| 출처 데이터셋 | uspto-grants-2014_11 |
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| ORD ID | ord-00fe353d2b4d45f4b86eb8337e7e6ede |
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| 출처 메모 | uspto-grants-2014_11 |
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