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HRID 487828作成日:2026年10月24日

17-Ethyl-1,14-dihydroxy-12-[1-(4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetrone → 17-Ethyl-1-hydroxy-12-[2-(4-hydroxy-3-methoxycyclo hexyl)-1-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetra methyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-14,18-diene-2.3,10,16-tetraone

https://huagongshe.com/ja/reaction/487828

反応式

関与物質

役割名称HCID仕込み量
反応物17-Ethyl-1,14-dihydroxy-12-[1-(4-hydroxy-3-methoxycyclohexyl)prop-1-en-2-yl]-23,25-dimethoxy-13,19,21,27-tetramethyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-18-ene-2,3,10,16-tetroneHCID 2241—
反応物p-Toluenesulfonic acidHCID 6101—
溶媒TolueneHCID 1140—
生成物17-Ethyl-1-hydroxy-12-[2-(4-hydroxy-3-methoxycyclo hexyl)-1-methylvinyl]-23,25-dimethoxy-13,19,21,27-tetra methyl-11,28-dioxa-4-azatricyclo[22.3.1.04,9]octacos-14,18-diene-2.3,10,16-tetraoneHCID 5728575181.9%

反応条件

温度100 °C

反応手順

17-Ethyl-1,14-dihydroxy-12-[2-(4-hydroxy-3-methoxycyclo hexyl)-1-methylvinyl)-23,25-dimethoxy-13,19,21,27-tetra methyl-11,28-dioxa-4-azatricyclo(22.3.1.04,9 ]octacos-18-ene-2,3,10,16-tetraone (FR-900520) (100 mg) and p-toluenesulphonic acid (2 mg) were dissolved in dry toluene (20 ml) and were heated for 2 hours at 100° C. under an atmosphere of nitrogen. Removal of solvent in vacuo and chromatography on silica eluting with hexane/acetone [2:1] gave the sub-title compound as a foam (80 mg).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05296489
出典データセットuspto-grants-1994_03
ORD IDord-9decd6b5e90d40f38a94ea670b681482
出典メモuspto-grants-1994_03