참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Morpholine | HCID 8083 | — |
| 반응물 | 6-Bromo-2-methyl-3-nitropyridine | HCID 24728014 | — |
| 용매 | Ethanol | HCID 702 | — |
| 생성물 | 4-(6-Methyl-5-nitro-2-pyridinyl)morpholine | HCID 8208955 | 69.7% |
반응 단계
To a solution of 6-bromo-2-methyl-3-nitropyridine (2.05 g, 9.45 mmol) in ethanol (10 mL) was added morpholine (1.728 mL, 19.84 mmol) and the reaction mixture was stirred at 70° C. for 5 hours. The reaction mixture was allowed to cool to room temperature causing a precipitate. The solid was collected by filtration and washed with ethanol (5 mL), then dried in vacuo. The crude was redissolved in a mixture of saturated sodium carbonate solution and ethyl acetate. The organic phase was separated, washed with further saturated sodium carbonate solution, then dried over magnesium sulphate and evaporated in vacuo to give the title compound (1.47 g) as a yellow solid. LCMS (2 min, formic) Rt 0.92 min, m/z (ES+) 224 (M+H).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09242972B2 |
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| 출처 데이터셋 | uspto-grants-2016_01 |
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| ORD ID | ord-456d0803c97f4b36b810f7a4623636de |
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| 출처 메모 | uspto-grants-2016_01 |
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