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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 340975생성일: 2026년 10월 24일

m-Chloroperbenzoic acid → (s)-Di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphate

https://huagongshe.com/ko/reaction/340975

반응식

참여 물질

역할이름HCID투입량
반응물m-Chloroperbenzoic acidHCID 70297—
반응물Di-tert-butyl N,N-DiisopropylphosphoramiditeHCID 853005—
반응물(S)-1-(1-(tert-butyldimethylsilyloxy)-5-hydroxypentan-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea (tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoateHCID 131729340—
반응물HCID 178418441HCID 178418441—
용매TetrahydrofuranHCID 8028—
생성물(s)-Di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphateHCID 5794750054%

반응 단계

To a solution of (S)-1-(1-(tert-butyldimethylsilyloxy)-5-hydroxypentan-2-yl)-3-(2,3-difluorobenzyl)-1-methylurea-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentanoate (6.1 g, 14.66 mmol) in THF (20 mL) was added tetrazole (0.34 M in acetonitrile, 172.0 mL, 58.64 mmol) followed by addition of di-tert-butyl diisopropylphosphoramidite (9.3 mL, 29.32 mmol) at RT The resulting solution was stirred at RT for 2 h. To this mixture was added MCPBA (70%, 7.3 g, 29.32 mmol) at RT. The reaction mixture was stirred at RT overnight and quenched with Na2SO3. The mixture was filtered and the filtrate was concentrated and dissolved in EtOAc. The organic mixture was washed with NaOH (1 N×2), NaHCO3 (sat.), and brine, dried over Na2SO4, filtered, and concentrated under reduced pressure. The residue was purified on silica gel column using a mixture of EtOAc and hexanes to give (S)-di-tert-butyl 5-(tert-butyldimethylsilyloxy)-4-(3-(2,3-difluorobenzyl)-1-methylureido)pentyl phosphate (4.1 g, 54%). LRMS (M+H+−2 tBu) m/z 491.2.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US08895582B2
출처 데이터셋uspto-grants-2014_11
ORD IDord-df3482bbd84f4c4682ed9f2168837b99
출처 메모uspto-grants-2014_11