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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1437811생성일: 2026년 10월 27일

Triethylamine → (1S)-3-[(2S,3R)-2-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-1-(4-iodophenyl)-4-oxoazetidin-3-yl]-1-(4-fluorophenyl)propyl acetate

https://huagongshe.com/reaction/1437811

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참여 물질

역할이름HCID투입량
반응물TriethylamineHCID 8471—
반응물tert-Butyldimethylsilyl trifluoromethanesulphonateHCID 123564—
반응물1-((1,1-Dimethylethyl)dimethylsilyl)-1H-imidazoleHCID 171385—
반응물(3R,4S)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)-1-(4-iodophenyl)azetidin-2-oneHCID 10098065—
용매DichloromethaneHCID 6344—
생성물(1S)-3-[(2S,3R)-2-(4-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-1-(4-iodophenyl)-4-oxoazetidin-3-yl]-1-(4-fluorophenyl)propyl acetateHCID 68975033—

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온도0 °C

반응 단계

To a solution of 0.5 g. (0.894 mmol, 1 equiv.) (3R,4S)-3-[(3S)-3-(4-fluorophenyl)-3-hydroxypropyl]-4-(4-hydroxyphenyl)-1-(4-iodophenyl)azetidin-2-one (i-6) in 5 mL anhydrous methylene chloride under inert atmosphere at 0° C. was added 0.36 mL (1.564 mmol, 1.75 equiv.) tert-butyldimethylsilyl trifluoromethanesulfonate, 0.175 mL (0.894 mmol, 1 equiv.) N-tert-butyldimethylsilylimidazole and 0.311 mL (2.234 mmol, 2.5 equivalents) triethylamine. The resulting reaction mixture was stirred at 0° C. for 15 minutes then quenched by the addition of 5 mL of sat. aq. solution of sodium carbonate. The resulting mixture was transferred to a separatory funnel, extracted with methylene chloride (3×5 mL). The combined organic extracts were dried over anhydrous Na2SO4 filtered and the solvent removed under vacuum. The residue was purified by prep. Tlc eluting with EtOAc/hexanes (2/1) to afford the title compound. m/z (ES) 696.0 (M+Na+), 614.0 (M−OAc+).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07622449B2
출처 데이터셋uspto-grants-2009_11
ORD IDord-099b69c9d5844e988b42a4973ad6ad47
출처 메모uspto-grants-2009_11