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HuagongsheHuagongshe Chemie-Druckbericht · Nur für Forschungszwecke
HRID 1450404Erstellt: 25. Oktober 2026

4-Bromoaniline → Ethyl 4'-[(5-Ethylpyrazolo[1,5-a]pyrimidine-7-yl)amino]biphenyl-2-carboxylate

https://huagongshe.com/reaction/1450404

Reaktionsgleichung

Beteiligte Stoffe

RolleNameHCIDEinwaage
Edukt4-BromoanilineHCID 7807—
EduktEthyl 2-bromobenzoateHCID 80186—
Edukt7-Chloro-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10535410—
EduktEthyl 4'-amino-biphenyl-2-carboxylateHCID 19975704—
LösungsmittelEthanolHCID 702—
ProduktEthyl 4'-[(5-Ethylpyrazolo[1,5-a]pyrimidine-7-yl)amino]biphenyl-2-carboxylateHCID 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

DOI10.6084/m9.figshare.5104873.v1
PatentnummerUS05602136
Quelldatensatzuspto-grants-1997_02
ORD IDord-f70a66bc973748cc95a2fbc9643d46fd
Quellennotizuspto-grants-1997_02