참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 4-Aminophenol | HCID 403 | — |
| 반응물 | Cesium carbonate | HCID 10796 | — |
| 반응물 | N-methyl-2-pyrrolidone | HCID 13387 | — |
| 반응물 | HCID 59351287 | HCID 59351287 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 1-(4-(3-(4-Aminophenoxy)pyrazin-2-yl)piperidin-1-yl)ethanone | HCID 59374162 | — |
반응 단계
1-(4-(3-fluoropyrazin-2-yl)piperidin-1-yl)ethanone (0.153 g, 0.685 mmol), 4-aminophenol (0.079 g, 0.720 mmol), cesium carbonate (0.246 g, 0.754 mmol), and 1-methyl-2-pyrrolidinone (0.685 mL, 0.685 mmol) were combined in a sealed tube and heated at 80° C. for 20 h. The cooled reaction mixture was diluted with EtOAc and washed with water; the aqueous layer was back-extracted with EtOAc (1×). The organic layers were combined, dried (MgSO4), filtered, and concentrated in vacuo. ISCO purification (20% to 80% EtOAc/Hexanes) afforded 1-(4-(3-(4-aminophenoxy)pyrazin-2-yl)piperidin-1-yl)ethanone as a light brown oil. MS (ESI, pos. ion) m/z: 313.0 (M+1).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08637500B2 |
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| 출처 데이터셋 | uspto-grants-2014_01 |
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| ORD ID | ord-309c1eeab3ee4f1b8e3e89c29bc0b0db |
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| 출처 메모 | uspto-grants-2014_01 |
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