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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 2352070Generated: November 1, 2026

Water → 1,1-Diethyl-3-(6-methyl-2-formyl-8alpha-ergolinyl)urea

https://huagongshe.com/reaction/2352070

Reaction equation

Participants

RoleNameHCIDCharge
ReactantWaterHCID 962—
ReactantPotassium CarbonateHCID 11430—
ReactantSulfuryl chlorideHCID 24648—
Reactant1,1-Diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8ergolinyl]ureaHCID 57025283—
SolventChloroformHCID 6212—
Product1,1-Diethyl-3-(6-methyl-2-formyl-8alpha-ergolinyl)ureaHCID 1574652261%

Reaction Steps

Under argon, 2.12 g (5 mmol) of 1,1-diethyl-3-[2-(1,3-dithiolan-2-yl)-6-methyl-8ergolinyl]urea is dissolved in 40 ml of chloroform. Then 3.5 g of silica gel is added and, under vigorous agitation, 3.5 ml of water is introduced dropwise. During a time period of 30 minutes, a solution of 1.18 ml of sulfuryl chloride in 30 ml of chloroform is added dropwise. After 3 hours of agitation at room temperature, 7.5 g of potassium carbonate is added and the mixture vigorously stirred for 20 minutes. The precipitate is filtered off and rinsed with chloroform. The precipitate is moistened with ethanol and introduced into 300 ml of saturated sodium chloride solution which is then repeatedly extracted with chloroform. The chloroform extracts and the chloroform filtrate are dried together over magnesium sulfate and evaporated. Subsequent crystallization takes place from ethyl acetate, thus isolating 1.16 g of 1,1-diethyl-3-(6-methyl-2-formyl-8α-ergolinyl)urea (61% yield).

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04874768
Source datasetuspto-grants-1989_10
ORD IDord-d3de9ca5b59b4728b0ca1f90a16f49ad
Source noteuspto-grants-1989_10