참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | 2,6-Dibromopyridine | HCID 12274 | — |
| 반응물 | (s)-1-(3-Nitrophenyl)ethanamine | HCID 11292459 | — |
| 반응물 | Bis(diphenylphosphino)-1,1'-binaphthyl | HCID 18630801 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 용매 | Toluene | HCID 1140 | — |
| 용매 | Ethyl Acetate | HCID 8857 | — |
| 생성물 | 6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amine | HCID 86641856 | 33% |
반응 단계
A mixture of (1S)-1-(3-nitrophenyl)ethanamine (365 mg, 2.2 mmol), 2,6-dibromopyridine (474 mg, 2 mmol), tris(dibenzylidene)dipalladium(0) (92 mg, 0.1 mmol), (+/−)-bis(diphenyphosphino)-1,1′-binaphthalene (125 mg, 0.2 mmol) and sodium tert-butoxide (270 mg, 2.8 mmol) in anhydrous toluene (4 mL) was heated at 80° C. for 17 hours. The mixture was cooled, diluted with ethyl acetate (50 mL), washed successively with saturated aqueous sodium hydrogen carbonate (3×30 mL) and brine (30 mL), dried (Na2SO4) and concentrated under reduced pressure to give a black oil which was purified by flash chromatography (silica, ethyl acetate/hexanes) to give 6-bromo-N-[(1S)-1-(3-nitrophenyl)ethyl]pyridin-2-amine (210 mg, 33%) and the di-addition product (205 mg, 50%) both as yellow oils.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US09029386B2 |
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| 출처 데이터셋 | uspto-grants-2015_05 |
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| ORD ID | ord-669d641cd5904fd7b163a83c97b03946 |
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| 출처 메모 | uspto-grants-2015_05 |
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