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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1280661Generated: November 2, 2026

Triethylamine → N-(tert-butyl)-N'-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]thiourea

https://huagongshe.com/reaction/1280661

Reaction equation

Participants

RoleNameHCIDCharge
ReactantTriethylamineHCID 8471—
Reactanttert-Butyl isothiocyanateHCID 11544—
ReactantHCID 22747878HCID 22747878—
SolventEthanolHCID 702—
ProductN-(tert-butyl)-N'-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]thioureaHCID 22747875—

Reaction Conditions

Temperature50 °C

Reaction Steps

11.2 cm3 of triethylamine are added with stirring to a solution of 7.91 g of (2RS)-2-amino-3-(2-pyrazinyl)-1-propanol dihydrochloride in 80 cm3 of ethanol, followed by addition of 7.2 cm3 of tert-butyl isothiocyanate. The mixture is heated at a temperature in the region of 50° C. for 18 hours. After cooling, the reaction medium is concentrated under reduced pressure (1 kPa) at a temperature in the region of 40° C., taken up in 100 cm3 of water and extracted with dichloromethane. The organic phases are combined, washed with 50 cm3 of water, dried over magnesium sulphate, filtered and then concentrated under reduced pressure (1 kPa) at a temperature in the region of 40° C. 7.2 g of N-(tert-butyl)-N′-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)-ethyl]thiourea are obtained in the form of a colourless paste [mass spectrum: DCI m/z=269 MH+]

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06451821B1
Source datasetuspto-grants-2002_09
ORD IDord-5e824b9edaec4e0c8311a531e461a1fa
Source noteuspto-grants-2002_09