HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 911057Generated: November 1, 2026
Triethylamine → 4-(4-methoxybenzylthio)-5-bromo-N-(4-phenethylthiazol-2-yl)pyridine-2-amine
https://huagongshe.com/reaction/911057
Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-4-phenylbutan-2-one | HCID 12608027 | — |
| Reactant | 1-(4-(4-Methoxybenzylthio)-5-bromopyridin-2-yl)thiourea | HCID 86634771 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | 4-(4-methoxybenzylthio)-5-bromo-N-(4-phenethylthiazol-2-yl)pyridine-2-amine | HCID 86634772 | 61% |
Reaction Steps
1-(4-(4-methoxybenzylthio)-5-bromopyridin-2-yl)thiourea (3.0 g, 7.8 mmol) and 1-bromo-4-phenylbutan-2-one (1.77 g, 7.8 mmol) were diluted in EtOH (120 mL). Triethylamine (2.2 ml, 15.6 mmol) was added, and the solution was heated at 75° C. for 3 hours. The solution was cooled and concentrated to half the amount of solvent. The solid was filtered and rinsed with cold EtOH to provide the desired product (2.44 g, 61% yield) as a tan solid.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08022222B2 |
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| Source dataset | uspto-grants-2011_09 |
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| ORD ID | ord-defef47dc77b4ab9a4f0882c90c4e60b |
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| Source note | uspto-grants-2011_09 |
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