Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Triethylamine | HCID 8471 | — |
| Reactant | 1-Bromo-4-phenylbutan-2-one | HCID 12608027 | — |
| Reactant | 1-(4-(Benzyloxy)-5-bromopyridin-2-yl)thiourea | HCID 86634776 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 86634777 | HCID 86634777 | 78.7% |
Reaction Steps
A flask was charged with 1-(4-(benzyloxy)-5-bromopyridin-2-yl)thiourea (2.34 g, 6.92 mmol), 1-bromo-4-phenylbutan-2-one (1.65 g, 7.26 mmol), and triethylamine (1.93 ml, 13.8 mmol). Ethanol (100 mL) was added and the reaction was stirred at 75° C. for 8 hours. The reaction was cooled and filtered, and the collected solids were washed with water to give the desired product (2.54 g, 77.9% yield) as a white 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-4faf7bc11e414e8ab07b3fc95f8ae7ef |
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| Source note | uspto-grants-2011_09 |
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