Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | P-Cresol | HCID 2879 | — |
| Reactant | Cesium carbonate | HCID 10796 | — |
| Reactant | 2(1H)-Pyrimidinone, tetrahydro-1,3-dimethyl- | HCID 81646 | — |
| Solvent | Water | HCID 962 | — |
| Product | HCID 57782331 | HCID 57782331 | — |
Reaction Steps
A mixture of the compound obtained in Example 1-(1) (30.27 g), 4-cresol (17.69 g), Cs2CO3 (53.43 g) and N,N′-dimethylpropyleneurea (DMPU) (136 ml) was stirred at 200° C. for 3 hours. The mixture was cooled to room temperature, diluted with water, and extracted with AcOEt. After washing with brine, the organic layer was dried over MgSO4, filtered and evaporated under reduced pressure to remove the solvent. The resulting crude product was purified by column chromatography (neutral OH-type SiO2, hexane/AcOEt=10% to 40%) to give the titled compound (8.54 g, yellow oil).
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US07994204B2 |
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| Source dataset | uspto-grants-2011_08 |
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| ORD ID | ord-f0e1b8c5371c4801aedb3598c54f50eb |
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| Source note | uspto-grants-2011_08 |
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