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HRID 231713作成日:2026年10月23日

Ammonia → 3-[9,10-Didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]-1,1-diethylurea

https://huagongshe.com/ja/reaction/231713

反応式

関与物質

役割名称HCID仕込み量
反応物AmmoniaHCID 222—
反応物Ethyl formateHCID 8025—
反応物LisurideHCID 28864—
反応物1,1-EthanedithiolHCID 33645—
触媒Titanium TetrachlorideHCID 24193—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物3-[9,10-Didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]-1,1-diethylureaHCID 8674205512%

反応手順

Under argon, 11.5 g (0.03 mol) of 3-(9,10-didehydro-6-methyl-8α-ergolinyl)-1,1-diethylurea is dissolved in 300 ml of chloroform. At room temperature, 105 ml of ethyl formate and 5.4 ml of ethanedithiol are added in succession. Then 13.2 ml of titanium(IV) chloride in 150 ml of chloroform is added dropwise. The mixture is agitated for 3 days at room temperature. To work up the mixture, it is cooled in an ice bath and 75 ml of methanol and 600 ml of water are added in sequence dropwise to this mixture. The solution is rendered alkaline with 60 ml of 25% ammonia solution and extracted with methylene chloride. The organic phases are washed with water and dried over magnesium sulfate. The concentrated residue is chromatographed under pressure on silica gel with ethyl acetate/methanol 95:5, thus isolating 1.7 g of 3-[9,10-didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8α-ergolinyl]-1,1-diethylurea (12% yield).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US04847262
出典データセットuspto-grants-1989_07
ORD IDord-0bd8e2a6c5414cce8d6f8ddc70fc0fb6
出典メモuspto-grants-1989_07