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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 35215Generated: October 26, 2026

Dimethyl Sulfide → 3-(6-Methyl-13-nitro-8beta-ergolinyl)-1,1-diethylurea

https://huagongshe.com/reaction/35215

Reaction equation

Participants

RoleNameHCIDCharge
ReactantDimethyl SulfideHCID 1068—
ReactantTriethylamineHCID 8471—
ReactantTert-Butyl hypochloriteHCID 521297—
ReactantSodium ethoxideHCID 2723922—
Reactant3-(2,3-Dihydro-6-methyl-13-nitro-8beta-ergolinyl)-1,1-diethylureaHCID 86742352—
SolventEthanolHCID 702—
SolventWaterHCID 962—
SolventDichloromethaneHCID 6344—
Product3-(6-Methyl-13-nitro-8beta-ergolinyl)-1,1-diethylureaHCID 8674235125.9%

Reaction Steps

A solution of 0.4 mmol of tert-butyl hypochlorite in 2 ml of methylene chloride is added dropwise to a solution of 0.3 mmol of 3-(2,3-dihydro-6-methyl-13-nitro-8β-ergolinyl)-1,1-diethylurea, 0.4 mmol of dimethyl sulfide, and 0.3 mmol of triethylamine in 5 ml of methylene choride at -70° C., and the mixture is agitated for 2 hours. Then a solution of 2 mmol of sodium ethylate in 2 ml of ethanol is added thereto within 10 minutes, and the mixture is warmed up to room temperature within 2 hours, whereafter it is combined with water, extracted with methylene chloride, the organic phase is dried and evaporated. Chromatography on silica gel with methylene chloride/methanol (5%) yields 30 mg of 3-(6-methyl-13-nitro-8β-ergolinyl)-1,1-diethylurea.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04766128
Source datasetuspto-grants-1988_08
ORD IDord-b8a17eee9b8649738d7245eacbbd1a9e
Source noteuspto-grants-1988_08