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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 17140생성일: 2026년 10월 25일

N-Iodosuccinimide → 7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amine

https://huagongshe.com/reaction/17140

반응식

참여 물질

역할이름HCID투입량
반응물N-IodosuccinimideHCID 120273—
반응물3-(4-Phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 18450763—
용매DimethylformamideHCID 6228—
생성물7-Iodo-3-(4-phenoxyphenyl)thieno[3,2-c]pyridin-4-amineHCID 1845087875%

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

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07737160B2
출처 데이터셋uspto-grants-2010_06
ORD IDord-dff3e8914e1642b09fc7349c0c1f1600
출처 메모uspto-grants-2010_06