참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | N-Iodosuccinimide | HCID 120273 | — |
| 반응물 | 3-(4-Phenoxyphenyl)thieno[3,2-c]pyridin-4-amine | HCID 18450763 | — |
| 용매 | Dimethylformamide | HCID 6228 | — |
| 생성물 | 7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amine | HCID 18450878 | 75% |
반응 단계
A solution of Example 219B (5 g, 15.7 mmol) in DMF (100 mL) was treated with N-iodosuccinimide (4.23 g, 18.8 mmol), stirred at ambient temperature for 2 hours, concentrated to half the original volume, and poured into 5% sodium thiosulfate (400 mL). The mixture was filtered and the filter cake was washed with water and dried. The solids were dissolved in dichloromethane (300 mL), treated with silica gel (80 g), and concentrated. The residue was transferred to a silica gel column (600 g) and chromatographed with ethyl acetate/heptane (1:6) to provide 5.2 g (75%) of the desired product. 1H NMR (CD2Cl2, 400 MHz) δ 7.95 (s, 1H), 7.33-7.29 (m, 4H), 7.12 (s, 1H), 7.10 (t, 1H), 7.02-6.99 (m, 4H), 4.76 (br s, 1H); 13C NMR (CD2Cl2, 400 MHz) δ 158.4, 156.8, 154.7, 154.4, 148.6, 138.4, 131.3, 131.2, 130.4, 124.4, 122.9, 120.0, 119,9, 118.8, 72.0.
출처 및 근거
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US07737160B2 |
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| 출처 데이터셋 | uspto-grants-2010_06 |
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| ORD ID | ord-dff3e8914e1642b09fc7349c0c1f1600 |
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| 출처 메모 | uspto-grants-2010_06 |
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