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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35850Generated: October 25, 2026

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

https://huagongshe.com/reaction/35850

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantEthyl formateHCID 8025—
Reactant1,1-EthanedithiolHCID 33645—
Reactant1,1-Diethyl-3-(2,6-dimethyl-8alpha-ergolinyl)ureaHCID 14011011—
CatalystTitanium TetrachlorideHCID 24193—
SolventMethanolHCID 887—
SolventWaterHCID 962—
SolventChloroformHCID 6212—
SolventDichloromethaneHCID 6344—
Product1,1-Diethyl-3-[13-(1,3-dithiolan-2-yl)-2,6-dimethyl-8alphaergolinyl]-ureaHCID 86748652—

Reaction Steps

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).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411966
Source datasetuspto-grants-1995_05
ORD IDord-fa9675f3aadc48238365a85657fbe7e7
Source noteuspto-grants-1995_05