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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 500817생성일: 2026년 10월 25일

3-Fluoro-4-(2-(4-(methylsulfonyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)benzenamine → N-(3-Fluoro-4-(2-(4-hydroxyphenyl)thieno[3,2-b]pyridin-7-yloxy)phenylcarbamothioyl)-2-phenylacetamide

https://huagongshe.com/reaction/500817

반응식

참여 물질

역할이름HCID투입량
반응물3-Fluoro-4-(2-(4-(methylsulfonyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)benzenamineHCID 58772869—
반응물N-(3-Fluoro-4-(2-(4-(methylsulfonyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)phenylcarbamothioyl)-2-phenylacetamideHCID 58772875—
반응물4-(7-(4-Amino-2-fluorophenoxy)thieno[3,2-b]pyridin-2-yl)phenolHCID 136059647—
생성물N-(3-Fluoro-4-(2-(4-hydroxyphenyl)thieno[3,2-b]pyridin-7-yloxy)phenylcarbamothioyl)-2-phenylacetamideHCID 1363351773%

반응 단계

Following the procedure described above for the synthesis of Compound 50 (Scheme 10, Example 55) but substituting amine 49 for the amine 154, title Compound 155a was obtained in 3% yield. Characterization of 155a is provided in the Table 14a.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07772247B2
출처 데이터셋uspto-grants-2010_08
ORD IDord-4e9740a78ba24da3b672d113b58ba882
출처 메모uspto-grants-2010_08