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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2193688생성일: 2026년 10월 27일

Stannous Chloride → 4-(2-(4-(((2-Chloroethyl)(methyl)amino)methyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorobenzenamine

https://huagongshe.com/reaction/2193688

반응식

참여 물질

역할이름HCID투입량
반응물Stannous ChlorideHCID 24479—
반응물2-Chloro-N-(4-(7-(2-fluoro-4-nitrophenoxy)thieno[3,2-b]pyridin-2-yl)benzyl)-N-methylethanamineHCID 58790204—
용매MethanolHCID 887—
생성물4-(2-(4-(((2-Chloroethyl)(methyl)amino)methyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorobenzenamineHCID 58790153100%

반응 단계

To a solution of 86 (375 mg, 0.79 mmol) in MeOH (15 ml) was added SnCl2×2H2O (891 mg, 5, eq, 3.95 mmol) and the reaction mixture was heated to reflux for 3 hours. The mixture was cooled to RT and poured onto ice/water then basified to pH 9. The mixture was filtered and the aqueous solution was extracted with EtOAc and the EtOAc was washed with brine solution. The organic phase was collected, dried over Na2SO4, filtered and concentrated and the 4-(2-(4-(((2-chloroethyl)(methyl)amino)methyl)phenyl)thieno[3,2-b]pyridin-7-yloxy)-3-fluorobenzenamine (87) (348 mg, 100% yield) was used immediately in the next step with no additional purification.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08329726B2
출처 데이터셋uspto-grants-2012_12
ORD IDord-203602c2bda34af1a7e13054a53cd419
출처 메모uspto-grants-2012_12