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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 2101222생성일: 2026년 10월 26일

Acetic Acid → Tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-hydroxyphenyl)-3-[(4-methoxybenzyl)thio]pentanoate

https://huagongshe.com/reaction/2101222

반응식

참여 물질

역할이름HCID투입량
반응물Acetic AcidHCID 176—
반응물3-(t-Butyldimethylsiloxy)iodobenzeneHCID 2757280—
반응물Tetrabutylammonium Fluoride TrihydrateHCID 11726816—
반응물Tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-3-[(4-methoxybenzyl)thio]pentanoateHCID 69072378—
용매TetrahydrofuranHCID 8028—
용매Ethyl AcetateHCID 8857—
생성물Tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-hydroxyphenyl)-3-[(4-methoxybenzyl)thio]pentanoateHCID 6907204198%

반응 단계

Glacial acetic acid (190 μL, 3.3 mmoL) was added to a solution of tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-{[tert-butyl(dimethyl)silyl]oxy}phenyl)-3-[(4-methoxybenzyl)thio]pentanoate (800 mg, 0.89 mmol, synthesised according to the procedure for Example 1, starting from tert-butyl(3-iodophenoxy)dimethylsilane) in dry THF (10 mL). Tetrabutylammonium fluoride trihydrate (489 mg, 1.5 mmol) was added and the mixture was stirred for 12 h at room temperature. EtOAc (150 mL) was added and the solution was washed with saturated aqueous NaHCO3, water and brine, dried and concentrated. Flash chromatography (CH2Cl2/EtOAc, 10:1) gave tert-butyl 2-({6-[(tert-butoxycarbonyl)amino]pyridin-3-yl}methyl)-5-(3-hydroxyphenyl)-3-[(4-methoxybenzyl)thio]pentanoate (660 mg, 98%).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07572817B2
출처 데이터셋uspto-grants-2009_08
ORD IDord-c307d529028143bbbf89ae522e45c921
출처 메모uspto-grants-2009_08