Participants
| Role | Name | HCID | Charge |
|---|
| Reactant | Methanol | HCID 887 | — |
| Reactant | 2,4-Difluorophenol | HCID 123051 | — |
| Reactant | HCID 57614141 | HCID 57614141 | — |
| Solvent | Dichloromethane | HCID 6344 | — |
| Product | HCID 57614150 | HCID 57614150 | — |
Reaction Steps
5-Chloro-6-(4-fluorophenyl)[1,3]thiazolo[5,4-d]pyrimidin-7(6H)-one (0.2 mmol) and 2.4-difluorophenol (0.4 mmol) are added to a vial, and the sealed mixture is heated with stirring at 140° C. for 48 h. Silica gel column chromatography (MeOH:CH2Cl2=0.5:99.5) gives the title compound as a slightly yellow solid. 1H NMR (400 MHz, CDCl3) 8.70 (1H, s), 7.36 (2H, m), 7.26 (2H, m), 7.14 (1H, m), 6.94 (2H, m). MS (M+1): 376.03; RT=1.33 min.
Provenance & Evidence
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patent number | US08759361B2 |
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| Source dataset | uspto-grants-2014_06 |
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| ORD ID | ord-a400e35dbac7457998fa9ef15eca839e |
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| Source note | uspto-grants-2014_06 |
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