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HRID 231713Erstellt: 24. Oktober 2026

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

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

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
EduktAmmoniaHCID 222—
EduktEthyl formateHCID 8025—
EduktLisurideHCID 28864—
Edukt1,1-EthanedithiolHCID 33645—
KatalysatorTitanium TetrachlorideHCID 24193—
LösungsmittelMethanolHCID 887—
LösungsmittelWaterHCID 962—
LösungsmittelChloroformHCID 6212—
Produkt3-[9,10-Didehydro-2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]-1,1-diethylureaHCID 8674205512%

Reaktionsschritte

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).

Herkunft & Nachweise

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS04847262
Quelldatensatzuspto-grants-1989_07
ORD IDord-0bd8e2a6c5414cce8d6f8ddc70fc0fb6
Quellennotizuspto-grants-1989_07