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Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 132693생성일: 2026년 10월 26일

Triethyl Phosphate → (1S,5S)-{1-[5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-(diethoxy-phosphoryloxy)-hexylcarbamoyl]-2,2-diphenyl-ethyl}-carbamic acid methyl ester

https://huagongshe.com/reaction/132693

반응식

참여 물질

역할이름HCID투입량
반응물Triethyl PhosphateHCID 6535—
반응물Diethyl chlorophosphateHCID 13139—
반응물Sodium hydrideHCID 24758—
반응물Ppl-100HCID 513956—
용매TetrahydrofuranHCID 8028—
생성물(1S,5S)-{1-[5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-(diethoxy-phosphoryloxy)-hexylcarbamoyl]-2,2-diphenyl-ethyl}-carbamic acid methyl esterHCID 24778259—

반응 단계

The PL-100 compound (product of step F, 203 mg, 0.325 mmol) was dissolved in dry tetrahydrofuran (3 mL) and 0.2 mL triethylphosphate under N2 atmosphere. The mixture was stirred at this temperature for 15 min, followed by the addition of diethyl chlorophosphate (0.061 mL, 0.423 mmol). Sodium hydride (60% in mineral oil) (17 mg, 0.423 mmol) was added at 0° C. The solution was stirred for 1 h at 0° C. and 12 h at room temperature. 20 mL of Amberlite XAD-2 was added to the solution and the beads were thoroughly mixed with the solvent. To the mixture was added ice water 2 mL, and the THF evaporated off. The beads were then washed with distilled water 6 times 100 mL then extracted three times with ethyl acetate (30 mL). The combined phase was evaporated and the residue was dried under high vacuum. The crude product was purified by flash chromatography using ethyl acetate/hexane (8/2), then EtOAc 100% as eluent. The yield of this reaction is 152 mg 61%.

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US07388008B2
출처 데이터셋uspto-grants-2008_06
ORD IDord-9c53cf24c9234fbeb2854a48044f32ef
출처 메모uspto-grants-2008_06