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HRID 231709作成日:2026年10月26日

Ammonia → 1,1-Diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]urea

https://huagongshe.com/reaction/231709

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1,1-EthanedithiolHCID 33645—
反応物TergurideHCID 443951—
触媒Titanium TetrachlorideHCID 24193—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
生成物1,1-Diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]ureaHCID 8674205442%

反応手順

At room temperature under argon, 7 ml of ethyl formate and 3.6 ml (44 mmol) of ethanedithiol are added in succession to a solution of 6.8 g of 1,1-diethyl-3-(6-methyl-8α-ergolinyl)urea in 200 ml of chloroform. Thereafter 8.8 ml (80 mmol) of titanium(IV) chloride dissolved in 100 ml of chloroform is added gradually dropwise to the mixture. The latter is stirred for 20 hours at room temperature. Although the starting material is not as yet entirely converted at this point in time, the reaction mixture is worked up to avoid further formation of the disubstituted compound. For this purpose, the reaction mixture is cooled in an ice bath and combined, in sequence, dropwise with 50 ml of methanol and 40 ml of water. The mixture is then made alkaline with 25% ammonia solution and extracted with methylene chloride. The organic phases are washed with water and dried over magnesium sulfate. The evaporated residue is crystallized in boiling heat from methanol/ethyl acetate, thus obtaining 3.8 g of 1,1-diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8α-ergolinyl]urea (42% 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-f5f5ba45034d40d79cd3c367248f3e5e
出典メモuspto-grants-1989_07