참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Potassium Carbonate | HCID 11430 | — |
| 반응물 | 4-Chloro-N-methylpicolinamide | HCID 1476814 | — |
| 반응물 | Potassium bis(trimethylsilyl)amide | HCID 3251421 | — |
| 반응물 | 4-Amino-3-Nitrophenol | HCID 3758882 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 4-(4-amino-3-nitrophenoxy)-N-methylpicolinamide | HCID 17756497 | — |
반응 단계
A mixture containing 4-amino-3-nitrophenol (1 eq) and potassium bis(trimethylsilyl)amide (2 eq) was stirred in dimethylformamide for 2 hours at room temperature. To this mixture was added (4-chloro(2-pyridyl))-N-methylcarboxamide (1 eq) and potassium carbonate (1.2 eq) and stirred at 90° C. for 3 days. The reaction mixture was then concentrated and partitioned between ethyl acetate and water. The organic layer was separated and washed with brine, dried, filtered, and concentrated in vacuum to give brown solid. Purification on silica gel (2% triethyl amine/50% ethyl acetate in hexane) gave 4-[(4-amino-3-nitrophenyl)oxy]-N-methylpyridine-2-carboxamide as an orange solid. The product gave satisfactory NMR. HPLC, 3.39 min; MS: MH+=289.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07728010B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-65a843943d0c4b12b9c7ec01aa513cf4 |
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| 출처 메모 | uspto-grants-2010_06 |
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