Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|
| Edukt | Ethyl Acetoacetate | HCID 8868 | — |
| Edukt | 3-(3-chlorophenyl)-1H-pyrazol-5-amine | HCID 178507281 | — |
| Lösungsmittel | O-Xylene | HCID 7237 | — |
| Produkt | HCID 178429161 | HCID 178429161 | 88% |
Reaktionsschritte
A suspension of 3-(3-chlorophenyl)-1H-pyrazol-5-amine (10 g, 51.6 mmol) and ethyl 3-oxobutanoate (26.3 ml, 207 mmol) in o-xylene (200 mL) was heated at reflux (oil bath temp: 155-160° C.) for 20 h. Note: The reaction turned clear solution between 60-70° C. and solids started crashing out at 130° C. Then, cooled, diluted with hexanes (100 mL), filtered, washed with hexanes (100 mL) and dried to afford 2-(3-chlorophenyl)-5-methylpyrazolo[1,5-a]pyrimidin-7-ol (11.8 g, 45.4 mmol, 88% yield) as off-white solid. 1H NMR (400 MHz, DMSO-d6) δ: 12.46 (s, 1H), 8.05 (s, 1H), 8.00-7.95 (m, 1H), 7.56-7.45 (m, 2H), 6.70 (s, 1H), 5.64 (s, 1H), 2.33 (s, 3H). LCMS (M+H) calcd for C13H11ClN6O: 260.06. found: 260.1.
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
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| Patentnummer | US08633200B2 |
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| Quelldatensatz | uspto-grants-2014_01 |
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| ORD ID | ord-9878c0973b224a8ba36dec8bb73a6da1 |
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| Quellennotiz | uspto-grants-2014_01 |
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