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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35851Generated: October 26, 2026

Ammonia → 2-Bromo-8alpha-(3,3-diethylureido)-6-methyl-ergoline-13-carbaldehyde

https://huagongshe.com/reaction/35851

Reaction equation

Participants

RoleNameHCIDCharge
ReactantAmmoniaHCID 222—
Reactant2,3-Dihydroxybutanedioic AcidHCID 875—
ReactantMethane, dichloromethoxy-HCID 21004—
ReactantAluminum(III) ChlorideHCID 6451240—
Reactant3-(2-Bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylureaHCID 13059860—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product2-Bromo-8alpha-(3,3-diethylureido)-6-methyl-ergoline-13-carbaldehydeHCID 86748653—

Reaction Steps

838 mg of 3-(2-bromo-6-methyl-8alpha-ergolinyl)-1,1-diethylurea (2 mmol) is dissolved in 100 ml of dichloromethane, 1.2 g of anhydrous aluminum chloride (9 mmol) and 1.8 ml of dichloromethyl methyl ether (20 mmol) are added and stirred for 15 minutes at room temperature. The reaction mixture is mixed with ice and, after 15 minutes, with a solution of 1.5 g of tartaric acid in 50 ml of water and made alkaline with 5 ml of conc. ammonia solution. It is extracted with dichloromethane, the organic phases are dried with sodium sulfate and the solvent is distilled off. The residue is chromatographed on silica gel with dichloromethane/methanol, 406 mg (45% of theory) is isolated.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS05411966
Source datasetuspto-grants-1995_05
ORD IDord-8ac1f04fc7bf4b3182f969b016355951
Source noteuspto-grants-1995_05