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HRID 473216作成日:2026年10月25日

Toluene → 8-Cyclopropyl-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline

https://huagongshe.com/reaction/473216

反応式

関与物質

役割名称HCID仕込み量
反応物TolueneHCID 1140—
反応物Potassium Phosphate, TribasicHCID 62657—
反応物Cyclopropylboronic acidHCID 2760897—
反応物8-Bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazolineHCID 66609469—
触媒Dichlorobis(tricyclohexylphosphine)pallium (II)HCID 11050900—
溶媒WaterHCID 962—
生成物8-Cyclopropyl-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazolineHCID 6660981684%

反応条件

温度100 °C

反応手順

To a mixture of 8-bromo-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline from Example 35 step B (200 mg, 0.5 mmol), dichlorobis(tricyclohexylphosphine)palladium(II) (37 mg, 0.05 mmol), cyclopropylboronic acid (65 mg, 0.75 mmol) and K3PO4 (371 mg, 1.75 mmol) were added toluene (6 mL) and water (0.5 mL). The reaction vessel was evacuated and flushed with argon (3×), and then the mixture was heated at 100° C. for 4 h. The mixture was concentrated under reduced pressure onto Celite and the residue was purified by silica gel chromatography eluting with 10-50% EtOAc/hexanes to afford impure 8-cyclopropyl-2-(difluoro(5-fluoropyridin-2-yl)methyl)-4-(methylthio)quinazoline (150 mg, 84%) which was used without further purification.

情報源と証拠

DOI10.6084/m9.figshare.5104873.v1
特許番号US08633207B2
出典データセットuspto-grants-2014_01
ORD IDord-4b691892610748fdaab7fcdc1a140446
出典メモuspto-grants-2014_01