Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Piperazine | HCID 4837 | — |
| Reactant | HCID 22349860 | HCID 22349860 | — |
| Solvent | Ethanol | HCID 702 | — |
| Product | HCID 22349876 | HCID 22349876 | 82.4% |
Reaction Steps
6.3 g of piperazine (73.5 mmol) were dissolved in 50 ml of ethanol. 2.31 g of 2-tert-butyl-4-chloro-6-difluoromethyl-pyrimidine (10.5 mmol) were added and the mixture was stirred for 3 h at 78° C. The solvent was evaporated and the residue was added slowly to 100 ml of water. After cooling, the pH was adjusted to 12 with 2 N aqueous sodium hydroxide, and aqueos layer was extracted with dichloromethane. The organic layer was dried over magnesium sulfate, filtered and the solvent was evaporated to yield 2.34 g of the title compound.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US06919342B2 |
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| Source dataset | uspto-grants-2005_07 |
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| ORD ID | ord-6cd42610f81f4a068a02be886b534a00 |
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| Source note | uspto-grants-2005_07 |
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