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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 272290생성일: 2026년 10월 26일

Water → Dimethyl 7-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-3-t-butoxycarbonylamino-3-hydroxymethylheptylphosphonate

https://huagongshe.com/reaction/272290

반응식

참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물TBAF tetrahydrofuranHCID 11078149—
반응물Dimethyl 7-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-3-t-butoxycarbonylamino-3-t-butyldimethylsiloxymethyl-1-heptenylphosphonateHCID 131727196—
용매TetrahydrofuranHCID 8028—
생성물Dimethyl 7-[4-(3-benzyloxyphenylthio)-2-chlorophenyl]-3-t-butoxycarbonylamino-3-hydroxymethylheptylphosphonateHCID 23094230—

반응 단계

The compound of Example 287 was reduced in the same manner as in Reference Example 123 and the resulting compound (107 mg) was dissolved in tetrahydrofuran (5.0 mL). A 1 mol/L TBAF-tetrahydrofuran solution (160 μL) was added dropwise and the mixture was stirred for 3 hours at room temperature. Subsequently, water was added and the reaction mixture was extracted with ethyl acetate. The extract was washed sequentially with water and a saturated aqueous solution of sodium chloride and the organic phase was dried over anhydrous sodium sulfate. The solvent was removed by distillation and the residue was purified on a silica gel column chromatography (ethyl acetate only) to obtain the desired product as a colorless oil (47 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07456157B2
출처 데이터셋uspto-grants-2008_11
ORD IDord-962c50109af24cc18087ea9ddcff22ab
출처 메모uspto-grants-2008_11