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HRID 231713생성일: 2026년 10월 23일

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

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

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Ethyl formateHCID 8025—
반응물LisurideHCID 28864—
반응물1,1-EthanedithiolHCID 33645—
촉매Titanium TetrachlorideHCID 24193—
용매MethanolHCID 887—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물3-[9,10-Didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]-1,1-diethylureaHCID 8674205512%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847262
출처 데이터셋uspto-grants-1989_07
ORD IDord-0bd8e2a6c5414cce8d6f8ddc70fc0fb6
출처 메모uspto-grants-1989_07