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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 720956생성일: 2026년 10월 25일

Water → (5S)-5-(acetylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-3-yl methyl hydrogen phosphate

https://huagongshe.com/reaction/720956

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참여 물질

역할이름HCID투입량
반응물WaterHCID 962—
반응물Methyl dichlorophosphateHCID 69611—
반응물(2R,3R,4S,5R,6R)-2-[(5S)-5-(Acetylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-3-yl]oxy-3,5-bis(isobutyryloxy)-6-[(isobutyryloxy)methyl]tetrahydro-2H-pyran-4-yl 2-methylpropanoateHCID 69586443—
용매TetrahydrofuranHCID 8028—
생성물(5S)-5-(acetylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-3-yl methyl hydrogen phosphateHCID 5865862769%

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온도0 °C

반응 단계

A solution of N-acetyl-colchicinol (1) (0.45 g; 1.26 mmol) in THF (40 ml) under argon was cooled to 0° C. and treated with a 1.0M solution of lithiumHMDS in THF (1.39 ml; 1.39 mmol). The mixture was stirred at 0° C. for 1 hour and then added in portions over about 15 minutes to a solution of methyl dichlorophosphate (625 μl; 4.16 mmol) in THF (150 ml). The mixture was stirred at ambient temperature for 15 minutes. After addition of water (200 ml) the THF was removed by evaporation. After removal of the insoluble material by filtration, the filtrate was purified on HP20 SS resin eluting with a gradient of 0–60% methanol/water. The appropriate fractions were freeze-dried to give (5S)-5-(acetylamino)-9,10,11-trimethoxy-6,7-dihydro-5H-dibenzo[a,c]cyclohepten-3-yl methyl hydrogen phosphate as white solid (391 mg).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07135502B1
출처 데이터셋uspto-grants-2006_11
ORD IDord-80655e5fe50041dcb93e915923ad6ca4
출처 메모uspto-grants-2006_11