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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 902955생성일: 2026년 10월 25일

Bromotrimethylsilane → N-[1-Carboxy-2-(1H-indol-3-yl)-ethyl]-3-(4-phenyl-2-phosphono-butyrylamino]-succinamic acid

https://huagongshe.com/reaction/902955

반응식

참여 물질

역할이름HCID투입량
반응물BromotrimethylsilaneHCID 76113—
반응물N-[1-benzyloxycarbonyl-2-(1H-indol-3-yl)-ethyl]-3-[2-(diethoxy-phosphoryl)4-phenyl-butyrylamino]-succinamic acid benzyl esterHCID 87735201—
촉매PalladiumHCID 23938—
용매MethanolHCID 887—
용매DichloromethaneHCID 6344—
생성물N-[1-Carboxy-2-(1H-indol-3-yl)-ethyl]-3-(4-phenyl-2-phosphono-butyrylamino]-succinamic acidHCID 21957074—

반응 단계

The more polar peptide phosphonate of Example 159 (54 mg, 69 μmol) was dissolved in dry CH2Cl2 (2 mL) followed by the addition of TMSBr (73 μL, 552 μmol). The resulting pale yellow solution was stirred for 40 h. The volatile materials were evaporated in vacuum at room temperature and the obtained residue was suspended in a water/methanol mixture (20:1) and vigorously stirred for 2 h after which it was lyophilized to give the crude phosphonic acid intermediate. This crude product was taken up in methanol (5 mL) and treated with Pd/C powder (10%, 25 mg). The mixture was stirred under an H2 atmosphere (45 PSI) for 12 h and then the catalyst was removed by filtration through a celite pad. The resulting mixture was concentrated to give the crude title compound which was purified by HPLC.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07365091B2
출처 데이터셋uspto-grants-2008_04
ORD IDord-bf0970a6a1e444df91a78a27ecc1f827
출처 메모uspto-grants-2008_04