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HRID 1450378作成日:2026年10月25日

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

https://huagongshe.com/reaction/1450378

反応式

関与物質

役割名称HCID仕込み量
反応物4-BromoanilineHCID 7807—
反応物Ethyl 2-bromobenzoateHCID 80186—
反応物7-Chloro-5-ethylpyrazolo[1,5-a]pyrimidineHCID 10535410—
反応物Ethyl 4'-amino-biphenyl-2-carboxylateHCID 19975704—
溶媒EthanolHCID 702—
生成物Ethyl 4'-[(5-Ethylpyrazolo[1,5-a]pyrimidine-7-yl)amino]biphenyl-2-carboxylateHCID 19975762—

反応手順

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, J. 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, m.p. 223°-225° C.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US05602137
出典データセットuspto-grants-1997_02
ORD IDord-4499175f94414b4aa9171766f50c1ecd
出典メモuspto-grants-1997_02