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HRID 231709생성일: 2026년 10월 25일

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

https://huagongshe.com/reaction/231709

반응식

참여 물질

역할이름HCID투입량
반응물AmmoniaHCID 222—
반응물Ethyl formateHCID 8025—
반응물1,1-EthanedithiolHCID 33645—
반응물TergurideHCID 443951—
촉매Titanium TetrachlorideHCID 24193—
용매MethanolHCID 887—
용매WaterHCID 962—
용매ChloroformHCID 6212—
생성물1,1-Diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8alpha-ergolinyl]ureaHCID 8674205442%

반응 단계

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).

출처 및 근거

DOI10.6084/m9.figshare.5104873.v1
특허 번호US04847262
출처 데이터셋uspto-grants-1989_07
ORD IDord-f5f5ba45034d40d79cd3c367248f3e5e
출처 메모uspto-grants-1989_07