HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
4-Bromoaniline → Ethyl 4'-[(5-Ethylpyrazolo[1,5-a]pyrimidine-7-yl)amino]biphenyl-2-carboxylate
Beteiligte Stoffe
| Rolle | Name | HCID | Einwaage |
|---|---|---|---|
| Edukt | 4-Bromoaniline | HCID 7807 | — |
| Edukt | Ethyl 2-bromobenzoate | HCID 80186 | — |
| Edukt | 7-Chloro-5-ethylpyrazolo[1,5-a]pyrimidine | HCID 10535410 | — |
| Edukt | Ethyl 4'-amino-biphenyl-2-carboxylate | HCID 19975704 | — |
| Lösungsmittel | Ethanol | HCID 702 | — |
| Produkt | Ethyl 4'-[(5-Ethylpyrazolo[1,5-a]pyrimidine-7-yl)amino]biphenyl-2-carboxylate | HCID 19975762 | — |
Reaktionsschritte
A solution of 800 mg (4.4 mmol) 7-chloro-5-ethylpyrazolo[1,5-a]pyrimidine (Example 1, Step B) and 1.0 g (4.1 mmol) ethyl 4'-amino-biphenyl-2-carboxylate (prepared from protected 4-bromoaniline and ethyl 2-bromobenzoate by the method of J. C. Adrian, Jr., C. S. Wilcox, I. Am. Chem. Soc., 1989, 111, 8055) in 40 ml dry ethanol was heated with reflux for 5 h. After cooling to room temperature pale yellow crystals of the title compound precipitated, which were filtered by suction and recrystallized from ethanol,
Herkunft & Nachweise
| DOI | 10.6084/m9.figshare.5104873.v1 |
|---|---|
| Patentnummer | US05602136 |
| Quelldatensatz | uspto-grants-1997_02 |
| ORD ID | ord-f70a66bc973748cc95a2fbc9643d46fd |
| Quellennotiz | uspto-grants-1997_02 |