戻る
化工社化工社 化学情報印刷レポート · 研究参考用
HRID 1677216作成日:2026年10月27日

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

反応式

関与物質

役割名称HCID仕込み量
反応物Triethyl PhosphateHCID 6535—
反応物Diethyl chlorophosphateHCID 13139—
反応物Sodium hydrideHCID 24758—
反応物Ppl-100HCID 513956—
溶媒TetrahydrofuranHCID 8028—
生成物(1S,5S)-{1-[5-[(4-amino-benzenesulfonyl)-isobutyl-amino]-6-(diethoxy-phosphoryloxy)-hexylcarbamoyl]-2,2-diphenyl-ethyl}-carbamic acid methyl esterHCID 24778259—

反応手順

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%.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08008297B2
出典データセットuspto-grants-2011_08
ORD IDord-4ab3236e7efb4e9280ee79080b87fb7a
出典メモuspto-grants-2011_08