참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Bromobenzene | HCID 7961 | — |
| 반응물 | 2-Amino-6-methylpyridine | HCID 15765 | — |
| 반응물 | Sodium t-butoxide | HCID 23676156 | — |
| 용매 | Toluene | HCID 1140 | — |
| 생성물 | 6-methyl-N-phenylpyridin-2-amine | HCID 21993539 | 35.7% |
반응 단계
To a flask were added 2.2 g of 2-amino-6-methylpyridine, 3.1 g of bromobenzene, 2.7 g of sodium tert-butoxide, and 50 ml toluene. The mixture was purged thoroughly with nitrogen and 62 mg of 2,2′-bis(diphenylphosphino)-1,1′-binaphthalenehthalene and 22 mg of palladium acetate were added. The reaction mixture was heated to 10° C. for 16 hours, and then cooled to 22 C. After quenching with 50 ml water, the product was extracted with 20 ml ethyl acetate, and washed with 15 ml water. The product was extracted with 50 ml of 1M hydrochloric acid, and then basified with aqueous ammonium hydroxide. Following extraction with 20 ml ethyl acetate, the product was purified by silica gel chromatography using a gradient from 10% ethyl acetate in hexane to 15% ethyl acetate in hexane, resulting in 1.3 g of a yellow-orange oil.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07538931B2 |
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| 출처 데이터셋 | uspto-grants-2009_05 |
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| ORD ID | ord-6bddddf6475e4d0d9015f38bdd96fc70 |
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| 출처 메모 | uspto-grants-2009_05 |
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