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HRID 35850作成日:2026年10月26日

Ammonia → 1,1-Diethyl-3-[13-(1,3-dithiolan-2-yl)-2,6-dimethyl-8alphaergolinyl]-urea

https://huagongshe.com/reaction/35850

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1,1-Diethyl-3-(2,6-dimethyl-8alpha-ergolinyl)ureaHCID 14011011—
触媒Titanium TetrachlorideHCID 24193—
溶媒MethanolHCID 887—
溶媒WaterHCID 962—
溶媒ChloroformHCID 6212—
溶媒DichloromethaneHCID 6344—
生成物1,1-Diethyl-3-[13-(1,3-dithiolan-2-yl)-2,6-dimethyl-8alphaergolinyl]-ureaHCID 86748652—

反応手順

5.31 g of 1,1-diethyl-3-(2,6-dimethyl-8alpha-ergolinyl)-urea (15 mmol) is dissolved in 150 ml of chloroform and 50 ml of formic acid ethyl ester, 2.8 ml of ethanedithiol (33 mmol) and 60 ml of a 1 molar solution of titanium tetrachloride in dichloromethane (60 mmol) are added and stirred for 20 hours at room temperature. Then, it is mixed with 40 ml of methanol and 300 ml of water, made alkaline with 30 ml of 25% ammonia solution and shaken out with dichloromethane. The organic phases are dried with sodium sulfate, concentrated by evaporation and the residue is chromatographed on silica gel with dichloromethane/methanol. 4.14 g of substance, which crystallizes from ethyl acetate, is isolated, [α]D =-4° (0.5 % in chloroform).

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05411966
出典データセットuspto-grants-1995_05
ORD IDord-fa9675f3aadc48238365a85657fbe7e7
出典メモuspto-grants-1995_05