참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Boc-4-hydroxyaniline | HCID 2756771 | — |
| 반응물 | 4-Chloro-3-nitropyridin-2-amine | HCID 4071694 | — |
| 반응물 | Potassium tert-butoxide | HCID 23665647 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | Tert-butyl 4-(2-amino-3-nitropyridin-4-yloxy)phenylcarbamate | HCID 42626044 | 66.8% |
반응 단계
Tert-butyl 4-hydroxyphenylcarbamate (3.63 g, 17.4 mmol) was dissolved in dry DMF (150 mL). Potassium tert-butoxide (2.62 g, 23.4 mmol) was added and the stirring was continued for 30 minutes at room temperature. 4-Chloro-3-nitropyridin-2-amine (3.0 g, 17.3 mmol) was added as a solid in one portion and the reaction mixture was subsequently heated at 85° C. for 4 hours. The reaction mixture was cooled, diluted with ethyl acetate (800 ml) and washed with water (1×800 ml) and brine (2×800 ml). The organic layer was dried with magnesium sulphate and evaporated. The crude was chromatographed over silica (eluant ethyl acetate:cyclohexane 1:2) to yield 4.0 g (63% yield) of tert-butyl 4-(2-amino-3-nitropyridin-4-yloxy)phenylcarbamate.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08198279B2 |
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| 출처 데이터셋 | uspto-grants-2012_06 |
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| ORD ID | ord-6c1610a9e41443cfabb853775213c53b |
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| 출처 메모 | uspto-grants-2012_06 |
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