Huagongshe화공사 화학 정보 인쇄 보고서 · 연구 참고용
HRID 1677216생성일: 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/1677216
참여 물질
| 역할 | 이름 | HCID | 투입량 |
|---|
| 반응물 | Triethyl Phosphate | HCID 6535 | — |
| 반응물 | Diethyl chlorophosphate | HCID 13139 | — |
| 반응물 | Sodium hydride | HCID 24758 | — |
| 반응물 | Ppl-100 | HCID 513956 | — |
| 용매 | Tetrahydrofuran | HCID 8028 | — |
| 생성물 | (1S,5S)-{1-[5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-(diethoxy-phosphoryloxy)-hexylcarbamoyl]-2,2-diphenyl-ethyl}-carbamic acid methyl ester | HCID 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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| 특허 번호 | US08008297B2 |
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| 출처 데이터셋 | uspto-grants-2011_08 |
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| ORD ID | ord-4ab3236e7efb4e9280ee79080b87fb7a |
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| 출처 메모 | uspto-grants-2011_08 |
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