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HRID 64605作成日:2026年10月25日

p-Toluenesulfonic acid → Etoposide

https://huagongshe.com/reaction/64605

反応式

関与物質

役割名称HCID仕込み量
反応物p-Toluenesulfonic acidHCID 6101—
反応物NitromethaneHCID 6375—
反応物1,1-DimethoxyethaneHCID 10795—
反応物4-Demethylepipodophyllotoxin 7'-O-beta-D-glucopyranosideHCID 159949—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物EtoposideHCID 36462—

反応手順

1.5 g. of dry 4'-demethylepipodophyllotoxin-beta-D-glucoside was suspended in 30 ml. of nitromethane, and 6 ml. of acetaldehyde-dimethylacetal and 150 mg. of p-toluene-sulphonic acid was added. The mixture was stirred at room temperature in an atmosphere of nitrogen and in the absence of moisture for one hour. After this time, the initial suspension had turned into a clear solution, and no starting material could be detected in the thin layer chromatogram (silica gel plates, eluant: chloroform+6% of methanol). Working up was effected by diluting with 400 ml. of chloroform and shaking out three times with 25 ml. each of water. The crude material obtained after concentrating the dried organic phase by evaporation was subsequently chromatographed on 100 g. of silica gel "Merck" (grain size 0.05 to 0.2 mm.), whereby chloroform containing 6% of methanol was continuously used as eluant. 4'-demethylepipodophyllotoxin-beta-D-ethylidene-glucoside, which is uniform according to thin layer chromatography, was obtained. After recrystallization from methanol colorless crystals having a M.P. of 236°-251° C., [α ]D22 =-110.5° (c.=0.588 in chloroform), were obtained.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04609644
出典データセットuspto-grants-1986_09
ORD IDord-eb2ee955085243c680971b0331a05f57
出典メモuspto-grants-1986_09