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HRID 1984429作成日:2026年10月27日

Potassium Phosphate, Tribasic → 1-(4-chlorobutyl)-2-methyl-2H-pyrazolo[3,4-c]quinolin-4-amine

https://huagongshe.com/reaction/1984429

反応式

関与物質

役割名称HCID仕込み量
反応物Potassium Phosphate, TribasicHCID 62657—
反応物2-Aminophenylboronic acid hydrochlorideHCID 16427090—
反応物4-bromo-5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carbonitrileHCID 66958992—
触媒Palladium, tris[mu-[(1,2-eta:4,5-eta)-(1E,4E)-1,5-diphenyl-1,4-pentadien-3-one]]di-, compd. with trichloromethane (1:1)HCID 11029508—
溶媒TolueneHCID 1140—
生成物1-(4-chlorobutyl)-2-methyl-2H-pyrazolo[3,4-c]quinolin-4-amineHCID 5771750213.1%

反応条件

温度110 °C

反応手順

2-Aminophenylboronic acid hydrochloride (9.20 g, 53.0 mmol), potassium phosphate (28.0 g, 133 mmol), tris(dibenzylideneacetone)dipalladium(0) chloroform adduct (685 mg, 0.662 mmol), and bis[(2-diphenylphosphino)phenyl]ether (428 mg, 0.795 mmol) were added to a mixture of 4-bromo-5-(4-chlorobutyl)-1-methyl-1H-pyrazole-3-carbonitrile (7.30 g, 26.5 mmol) and powdered molecular sieves (1 g) in toluene (165 mL). Nitrogen was bubbled through the reaction mixture, and then the reaction was heated at 110° C. for 24 hours. The mixture was filtered through a layer of silica gel (eluting with 3:2 chloroform/methanol). The filtrate was concentrated under reduced pressure and dissolved in ethanol (130 mL). Hydrogen chloride (20 mL of a 4 M solution in ethanol) was added to the solution and the reaction was heated at reflux for two hours and allowed to cool to ambient temperature. The reaction was worked up as described in Part F of Example 19. After purification by chromatography on a HORIZON HPFC system, the solid was stirred in acetonitrile and filtered to provide 1.0 g of 1-(4-chlorobutyl)-2-methyl-2H-pyrazolo[3,4-c]quinolin-4-amine that was used in the next step. The filtrate was concentrated to provide an additional 4.0 g of product.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US07544697B2
出典データセットuspto-grants-2009_06
ORD IDord-b332ecaadee1476fa416cd92f9344e31
出典メモuspto-grants-2009_06