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
Participants
| Role | Name | HCID | Charge |
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| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | tert-Butyl isothiocyanate | HCID 11544 | — |
| Reactant | HCID 22747878 | HCID 22747878 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | N-(tert-butyl)-N'-[(1RS)-1-hydroxymethyl-2-(2-pyrazinyl)ethyl]thiourea | HCID 22747875 | — |
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
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06451821B1 |
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| Source dataset | uspto-grants-2002_09 |
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| ORD ID | ord-5e824b9edaec4e0c8311a531e461a1fa |
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| Source note | uspto-grants-2002_09 |
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