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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 45692생성일: 2026년 10월 24일

Trimethylphosphine → (E)-ethyl 3-(4-(4-(N-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)sulfamoyl)phenoxy)-3,5-difluorophenyl)-2-methylacrylate

https://huagongshe.com/ko/reaction/45692

반응식

참여 물질

역할이름HCID투입량
반응물TrimethylphosphineHCID 68983—
반응물(E)-ethyl 3-(4-(4-(N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)sulfamoyl)phenoxy)-3,5-difluorophenyl)-2-methylacrylateHCID 86672339—
용매WaterHCID 962—
용매TetrahydrofuranHCID 8028—
생성물(E)-ethyl 3-(4-(4-(N-(2-(2-(2-(2-aminoethoxy)ethoxy)ethoxy)ethyl)sulfamoyl)phenoxy)-3,5-difluorophenyl)-2-methylacrylateHCID 70906018101%

반응 단계

To a solution of (E)-ethyl 3-(4-(4-(N-(2-(2-(2-(2-azidoethoxy)ethoxy)ethoxy)ethyl)sulfamoyl)phenoxy)-3,5-difluorophenyl)-2-methylacrylate (169 mg, 0.28 mmol) in THF (6 ml) and water (0.6 mL) under nitrogen was added trimethylphosphine (26 mg, 0.34 mmol). After stirring for 3 hours, the solvents were removed at reduced pressure and. The residue was dissolved in water (5 mL) and extracted with EtOAc (3×25 mL). The combined organic layers were dried (Na2SO4) and concentrated to give the title compound (162 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08541448B2
출처 데이터셋uspto-grants-2013_09
ORD IDord-f0f35b582d2a47409c67cb13c6948bc4
출처 메모uspto-grants-2013_09