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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35860Generated: October 27, 2026

Ammonia → 1,1-Diethyl,3-(2,6,13-trimethyl-8alpha-ergolinyl)-thiourea

https://huagongshe.com/reaction/35860

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
ReactantPhosphorus oxychlorideHCID 24813—
ReactantPotassium ethylxanthateHCID 2735045—
Reactant1,1-Diethyl-3-(2,6,13-trimethyl-8alpha-ergolinyl)-ureaHCID 67788086—
SolventAcetonitrileHCID 6342—
SolventDichloromethaneHCID 6344—
Product1,1-Diethyl,3-(2,6,13-trimethyl-8alpha-ergolinyl)-thioureaHCID 8842317143%

Reaction Steps

0.5 M1 of freshly distilled phosphorus oxychloride (5.6 mmol) and 368 mg of 1,1-diethyl-3-(2,6,13-trimethyl-8alpha- ergolinyl)-urea (1 mmol) are dissolved in 20 ml of dichloromethane at -20° C. and the mixture is allowed to stir overnight at room temperature. The volatile portions are now drawn off in a vacuum, the residue is dissolved in 40 ml of acetonitrile and mixed with a solution of 0.8 g of potassium xanthate (5.6 mmol) in 80 ml of acetonitrile. It is stirred for 2 hours at room temperature, then ice and conc. ammonia solution are added and shaken out with dichloromethane. The organic phases are dried with sodium sulfate and concentrated by evaporation, the residue is chromatographed on silica gel with ethyl acetate and crystallized from ethyl acetate/diisopropyl ether, yield 43%.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411966
Source datasetuspto-grants-1995_05
ORD IDord-4719f764f83a4b1f9dce88191a7e0933
Source noteuspto-grants-1995_05