참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Sodium Carbonate | HCID 10340 | — |
| 반응물 | Triphenylphosphine | HCID 11776 | — |
| 반응물 | 6-chloro-4-N-(4-chlorophenyl)pyrimidine-2,4-diamine | HCID 1484285 | — |
| 반응물 | 5-Chloro-2-methoxyphenylboronic acid | HCID 2735751 | — |
| 촉매 | palladium(II) acetate | HCID 167845 | — |
| 용매 | Water | HCID 962 | — |
| 용매 | 1,2-Dimethoxyethane | HCID 8071 | — |
| 생성물 | 6-(5-Chloro-2-methoxy-phenyl)-N*4*-(4-chloro-phenyl)-pyrimidine-2,4-diamine | HCID 11439833 | 49.4% |
반응 단계
To a mixture of 6-chloro-N*4*-(4-chloro-phenyl)-pyrimidine-2,4-diamine (0.5 g, 1.96 mmol), 5-chloro-2-methoxy-phenyl boronic acid (0.73 g, 3.92 mmol), palladium (II) acetate (0.066 g, 0.294 mmol), and triphenylphosphine (0.154 g, 0.588 mmol) was added a solution of sodium carbonate (0.63 g, 5.88 mmol) dissolved in water (6 ml) followed by glyme (20 ml). The reaction mixture was stirred under an argon atmosphere at 90-95° C. for 18 hours. After cooling to room temperature, the mixture was filtered through a pad of celite under suction and concentrated. The residue was purified by flash chromatography on silica gel eluting with ethyl acetate-hexane (1:3) to provide the title compound (0.350 g, 49% yield) as a white powder. 1H NMR (CDCl3) δ 3.86 (s, 3H, CH3), 4.90 (s, 2H, NH2), 6.58 (s, 1H, NH), 6.71 (s, 1H, Ar), 6.91 (d, 1H, J=8.8 Hz, Ar), 7.32-7.41 (m, 5H, Ar), 7.87 (d, 1H, J=2.7 Hz, Ar).
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07419984B2 |
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| 출처 데이터셋 | uspto-grants-2008_09 |
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| ORD ID | ord-3cff5c96b7894489880218862199ea5a |
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| 출처 메모 | uspto-grants-2008_09 |
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